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Published in: Familial Cancer 3/2018

01-07-2018 | Original Article

Genotype phenotype correlation in Asian Indian von Hippel–Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma

Authors: Nilesh Lomte, Sanjeet Kumar, Vijaya Sarathi, Reshma Pandit, Manjunath Goroshi, Swati Jadhav, Anurag R. Lila, Tushar Bandgar, Nalini S. Shah

Published in: Familial Cancer | Issue 3/2018

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Abstract

The data in genotype-phenotype correlation in Indian von Hippel–Lindau (VHL) patients is limited. We have retrospectively studied 31 genetically proven VHL patients with pheochromocytoma/paraganglioma (PCC/PGL) from families and have reviewed the World literature on PCC/PGL in patients with large VHL deletions. Three patients had large deletions and 28 patients had other mutations [missense mutations in 25, 3 bp deletion in 2 and single bp duplication in one]. Unilateral PCC were significantly more common in patients with large VHL deletions whereas multiple PCC (bilateral PCC or PCC + sympathetic PGL) were significantly more common in those with other mutations. World literature review confirmed the rarity of PCC/PGL in patients with large deletions and we report the first definitive case of PCC associated with complete VHL deletion. Pancreatic neuroendocrine tumours were more common, often metastatic and the most common cause of death in our cohort. Our study had eight parent off-spring pairs from five families. The off-springs were significantly younger at presentation and had significantly higher number of PCC/PGL. In conclusion, PCC/PGL are rare in patients with large VHL deletions and if occur are most likely to be solitary. Patients with bilateral PCC or multifocal PCC/PGL are least likely to have large VHL deletions. Our study also provides additional evidence for existence of the phenomenon of anticipation in VHL syndrome.
Literature
2.
go back to reference Ong KR, Woodward ER, Killick P, Lim C, Macdonald F, Maher ER (2007) Genotype–phenotype correlations in von Hippel–Lindau disease. Hum Mutat 28(2):143–149CrossRefPubMed Ong KR, Woodward ER, Killick P, Lim C, Macdonald F, Maher ER (2007) Genotype–phenotype correlations in von Hippel–Lindau disease. Hum Mutat 28(2):143–149CrossRefPubMed
3.
go back to reference Maher ER, Yates JR, Harries R et al (1990) Clinical features and natural history of von Hippel–Lindau disease. Q J Med 77(283):1151–1163CrossRefPubMed Maher ER, Yates JR, Harries R et al (1990) Clinical features and natural history of von Hippel–Lindau disease. Q J Med 77(283):1151–1163CrossRefPubMed
4.
go back to reference Gläsker S, Neumann HPH, Koch CA, Vortmeyer AO (2000) Von Hippel–Lindau Disease. In: De Groot LJ, Chrousos G, Dungan K, Feingold KR, Grossman A, Hershman JM, Koch C, Korbonits M, McLachlan R, New M, Purnell J, Rebar R, Singer F, Vinik A (eds) Endotext [Internet]. MDText.com, Inc., South Dartmouth, MA Gläsker S, Neumann HPH, Koch CA, Vortmeyer AO (2000) Von Hippel–Lindau Disease. In: De Groot LJ, Chrousos G, Dungan K, Feingold KR, Grossman A, Hershman JM, Koch C, Korbonits M, McLachlan R, New M, Purnell J, Rebar R, Singer F, Vinik A (eds) Endotext [Internet]. MDText.com, Inc., South Dartmouth, MA
5.
6.
go back to reference Gossage L, Eisen T, Maher ER (2015) VHL, the story of a tumour suppressor gene. Nat Rev Cancer 15(1):55–64CrossRefPubMed Gossage L, Eisen T, Maher ER (2015) VHL, the story of a tumour suppressor gene. Nat Rev Cancer 15(1):55–64CrossRefPubMed
7.
go back to reference McNeill A, Rattenberry E, Barber R, Killick P, MacDonald F, Maher ER (2009) Genotype–phenotype correlations in VHL exon deletions. Am J Med Genet A 149A(10):2147–2151CrossRefPubMed McNeill A, Rattenberry E, Barber R, Killick P, MacDonald F, Maher ER (2009) Genotype–phenotype correlations in VHL exon deletions. Am J Med Genet A 149A(10):2147–2151CrossRefPubMed
8.
go back to reference Pandit R, Khadilkar K, Sarathi V, Kasaliwal R et al (2016) Germline mutations and genotype–phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. Eur J Endocrinol 175(4):311–323CrossRefPubMed Pandit R, Khadilkar K, Sarathi V, Kasaliwal R et al (2016) Germline mutations and genotype–phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. Eur J Endocrinol 175(4):311–323CrossRefPubMed
9.
go back to reference Vikkath N, Valiyaveedan S, Nampoothiri S et al (2015) Genotype–phenotype analysis of von Hippel–Lindau syndrome in fifteen Indian families. Fam Cancer 14(4):585–594CrossRefPubMed Vikkath N, Valiyaveedan S, Nampoothiri S et al (2015) Genotype–phenotype analysis of von Hippel–Lindau syndrome in fifteen Indian families. Fam Cancer 14(4):585–594CrossRefPubMed
10.
go back to reference Ebenazer A, Rajaratnam S, Pai R et al (2013) Detection of large deletions in the VHL gene using a real–time PCR with SYBR green. Fam Cancer 12(3):519–524CrossRefPubMed Ebenazer A, Rajaratnam S, Pai R et al (2013) Detection of large deletions in the VHL gene using a real–time PCR with SYBR green. Fam Cancer 12(3):519–524CrossRefPubMed
13.
go back to reference Schwarz JM, Cooper DN, Schuelke M et al (2014) MutationTaster2: mutation prediction for the deep–sequencing age. Nat Methods 11:361–362CrossRefPubMed Schwarz JM, Cooper DN, Schuelke M et al (2014) MutationTaster2: mutation prediction for the deep–sequencing age. Nat Methods 11:361–362CrossRefPubMed
15.
go back to reference Kumar P, Henikoff S, Ng PC (2009) Predicting the effects of coding nonsynonymous variants on protein function using the SIFT algorithm. Nat Protoc 4:1073–1081CrossRefPubMed Kumar P, Henikoff S, Ng PC (2009) Predicting the effects of coding nonsynonymous variants on protein function using the SIFT algorithm. Nat Protoc 4:1073–1081CrossRefPubMed
16.
go back to reference Stenson PD, Mort M, Ball EV et al (2014) The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine. Hum Genet 133:1–9CrossRefPubMed Stenson PD, Mort M, Ball EV et al (2014) The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine. Hum Genet 133:1–9CrossRefPubMed
17.
18.
go back to reference Gossage L, Pires DE, Olivera–Nappa Á (2014) An integrated computational approach can classify VHL missense mutations according to risk of clear cell renal carcinoma. Hum Mol Genet 15(22):5976–5988CrossRef Gossage L, Pires DE, Olivera–Nappa Á (2014) An integrated computational approach can classify VHL missense mutations according to risk of clear cell renal carcinoma. Hum Mol Genet 15(22):5976–5988CrossRef
19.
go back to reference Nordstrom–O’Brien M, van der Luijt RB, van Rooijen E et al (2010) Genetic analysis of von Hippel–Lindau disease. Hum Mutat 31(5):521–537PubMed Nordstrom–O’Brien M, van der Luijt RB, van Rooijen E et al (2010) Genetic analysis of von Hippel–Lindau disease. Hum Mutat 31(5):521–537PubMed
20.
go back to reference Wong M, Chu YH, Tan HL et al (2016) Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome. Chin J Cancer 35:79CrossRefPubMedPubMedCentral Wong M, Chu YH, Tan HL et al (2016) Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome. Chin J Cancer 35:79CrossRefPubMedPubMedCentral
21.
go back to reference Crossey PA, Richards FM, Foster K, Green JS et al (1994) Identification of intragenic mutations in the von Hippel–Lindau disease tumour suppressor gene and correlation with disease phenotype. Hum Mol Genet 3(8):1303–1308CrossRefPubMed Crossey PA, Richards FM, Foster K, Green JS et al (1994) Identification of intragenic mutations in the von Hippel–Lindau disease tumour suppressor gene and correlation with disease phenotype. Hum Mol Genet 3(8):1303–1308CrossRefPubMed
22.
go back to reference Chen F, Kishida T, Yao M, Hustad T, Glavac D et al (1995) Germline mutations in the von Hippel–Lindau disease tumor suppressor gene: correlations with phenotype. Hum Mutat 5(1):66–75CrossRefPubMed Chen F, Kishida T, Yao M, Hustad T, Glavac D et al (1995) Germline mutations in the von Hippel–Lindau disease tumor suppressor gene: correlations with phenotype. Hum Mutat 5(1):66–75CrossRefPubMed
23.
go back to reference Franke G, Bausch B, Hoffmann MM et al (2009) Alu Alu recombination underlies the vast majority of large VHL germline deletions: Molecularcharacterization and genotype–phenotype correlations in VHL patients. Hum Mutat 30(5):776–786CrossRefPubMed Franke G, Bausch B, Hoffmann MM et al (2009) Alu Alu recombination underlies the vast majority of large VHL germline deletions: Molecularcharacterization and genotype–phenotype correlations in VHL patients. Hum Mutat 30(5):776–786CrossRefPubMed
24.
go back to reference Hes F, Zewald R, Peeters T, Sijmons R et al (2000) Genotype–phenotype correlations in families with deletions in the von Hippel–Lindau (VHL) gene. Hum Genet 106(4):425–431CrossRefPubMed Hes F, Zewald R, Peeters T, Sijmons R et al (2000) Genotype–phenotype correlations in families with deletions in the von Hippel–Lindau (VHL) gene. Hum Genet 106(4):425–431CrossRefPubMed
25.
go back to reference Cybulski C, Krzystolik K, Murgia A, Górski B, Debniak T et al (2002) Germline mutations in the von Hippel–Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene. J Med Genet 39(7):E38CrossRefPubMedPubMedCentral Cybulski C, Krzystolik K, Murgia A, Górski B, Debniak T et al (2002) Germline mutations in the von Hippel–Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene. J Med Genet 39(7):E38CrossRefPubMedPubMedCentral
26.
go back to reference Rocha JC, Silva RL, Mendonça BB, Marui S et al (2003) High frequency of novel germline mutations in the VHL gene in the heterogeneous population of Brazil. J Med Genet 40(3):e31CrossRefPubMedPubMedCentral Rocha JC, Silva RL, Mendonça BB, Marui S et al (2003) High frequency of novel germline mutations in the VHL gene in the heterogeneous population of Brazil. J Med Genet 40(3):e31CrossRefPubMedPubMedCentral
27.
go back to reference Maranchie JK, Afonso A, Albert PS, Kalyandrug S et al (2004) Solid renal tumor severity in von Hippel–Lindau disease is related to germline deletion length and location. Hum Mutat 23(1):40–46CrossRefPubMed Maranchie JK, Afonso A, Albert PS, Kalyandrug S et al (2004) Solid renal tumor severity in von Hippel–Lindau disease is related to germline deletion length and location. Hum Mutat 23(1):40–46CrossRefPubMed
28.
go back to reference Hes FJ, van der Luijt RB, Janssen AL et al (2007) Frequency of Von Hippel–Lindau germline mutations in classic and non–classic Von Hippel–Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation–dependent probe amplification. Clin Genet 72(2):122–129CrossRefPubMed Hes FJ, van der Luijt RB, Janssen AL et al (2007) Frequency of Von Hippel–Lindau germline mutations in classic and non–classic Von Hippel–Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation–dependent probe amplification. Clin Genet 72(2):122–129CrossRefPubMed
29.
go back to reference Cascón A, Escobar B, Montero–Conde C et al (2007) Loss of the actin regulator HSPC300 results in clear cell renal cell carcinoma protection in Von Hippel–Lindau patients. Hum Mutat 28(6):613–621CrossRefPubMed Cascón A, Escobar B, Montero–Conde C et al (2007) Loss of the actin regulator HSPC300 results in clear cell renal cell carcinoma protection in Von Hippel–Lindau patients. Hum Mutat 28(6):613–621CrossRefPubMed
30.
go back to reference Huang JS, Huang CJ, Chen SK, Chien CC (2007) Associations between VHL genotype and clinical phenotype in familial von Hippel–Lindau disease. Eur J Clin Invest 37(6):492–500CrossRefPubMed Huang JS, Huang CJ, Chen SK, Chien CC (2007) Associations between VHL genotype and clinical phenotype in familial von Hippel–Lindau disease. Eur J Clin Invest 37(6):492–500CrossRefPubMed
31.
go back to reference Cho HJ, Ki CS, Kim JW (2009) Improved detection of germline mutations in Korean VHL patients by multiple ligation–dependent probe amplification analysis. J Korean Med Sci 24(1):77–83CrossRefPubMedPubMedCentral Cho HJ, Ki CS, Kim JW (2009) Improved detection of germline mutations in Korean VHL patients by multiple ligation–dependent probe amplification analysis. J Korean Med Sci 24(1):77–83CrossRefPubMedPubMedCentral
32.
go back to reference Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I et al (2009) Germline VHL gene mutations in Hungarian families with von Hippel–Lindau disease and patients with apparently sporadic unilateral pheochromocytomas. Eur J Endocrinol 161(3):495–502CrossRefPubMed Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I et al (2009) Germline VHL gene mutations in Hungarian families with von Hippel–Lindau disease and patients with apparently sporadic unilateral pheochromocytomas. Eur J Endocrinol 161(3):495–502CrossRefPubMed
33.
go back to reference Gomy I, Molfetta GA, de Andrade Barreto E et al (2010) Clinical and molecular characterization of Brazilian families with von Hippel–Lindau disease: a need for delineating genotype–phenotype correlation. Fam Cancer 9(4):635–642CrossRefPubMed Gomy I, Molfetta GA, de Andrade Barreto E et al (2010) Clinical and molecular characterization of Brazilian families with von Hippel–Lindau disease: a need for delineating genotype–phenotype correlation. Fam Cancer 9(4):635–642CrossRefPubMed
34.
go back to reference Wu P, Zhang N, Wang X, Ning X, Li T, Bu D et al (2012) Family history of von Hippel–Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients. J Hum Genet 57(4):238–243CrossRefPubMed Wu P, Zhang N, Wang X, Ning X, Li T, Bu D et al (2012) Family history of von Hippel–Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients. J Hum Genet 57(4):238–243CrossRefPubMed
35.
go back to reference Wang X, Zhang N, Ning X, Li T, Wu P, Peng S et al (2014) Higher prevalence of novel mutations in VHL gene in Chinese Von Hippel–Lindau disease patients. Urology 83(3):675-e1CrossRef Wang X, Zhang N, Ning X, Li T, Wu P, Peng S et al (2014) Higher prevalence of novel mutations in VHL gene in Chinese Von Hippel–Lindau disease patients. Urology 83(3):675-e1CrossRef
37.
go back to reference Kruizinga RC, Sluiter WJ, de Vries EG, Zonnenberg BA, Lips CJ et al (2013) Calculating optimal surveillance for detection of von Hippel–Lindau–related manifestations. Endocr Relat Cancer 21(1):63–71CrossRefPubMed Kruizinga RC, Sluiter WJ, de Vries EG, Zonnenberg BA, Lips CJ et al (2013) Calculating optimal surveillance for detection of von Hippel–Lindau–related manifestations. Endocr Relat Cancer 21(1):63–71CrossRefPubMed
38.
go back to reference Wittström E, Nordling M, Andréasson S (2014) Genotype–phenotype correlations, and retinal function and structure in von Hippel–Lindau disease. Ophthalmic Genet 35(2):91–106CrossRefPubMed Wittström E, Nordling M, Andréasson S (2014) Genotype–phenotype correlations, and retinal function and structure in von Hippel–Lindau disease. Ophthalmic Genet 35(2):91–106CrossRefPubMed
39.
go back to reference Krzystolik K, Jakubowska A, Gronwald J et al (2014) Large deletion causing von Hippel–Lindau disease and hereditary breast cancer syndrome. Hered Cancer Clin Pract 12(1):16CrossRefPubMedPubMedCentral Krzystolik K, Jakubowska A, Gronwald J et al (2014) Large deletion causing von Hippel–Lindau disease and hereditary breast cancer syndrome. Hered Cancer Clin Pract 12(1):16CrossRefPubMedPubMedCentral
40.
go back to reference Ning XH, Zhang N, Li T, Wu PJ, Wang X, Li XY et al (2014) Telomere shortening is associated with genetic anticipation in Chinese Von Hippel–Lindaudisease families. Cancer Res 74(14):3802–3809CrossRefPubMed Ning XH, Zhang N, Li T, Wu PJ, Wang X, Li XY et al (2014) Telomere shortening is associated with genetic anticipation in Chinese Von Hippel–Lindaudisease families. Cancer Res 74(14):3802–3809CrossRefPubMed
41.
go back to reference Lee JS, Lee JH, Lee KE, Kim JH, Hong JM, Ra EK et al (2016) Genotype–phenotype analysis of von Hippel–Lindau syndrome in Korean families: HIFα bindingsite missense mutations elevate age–specific risk for CNS hemangioblastoma. BMC Med Genet 17(1):48CrossRefPubMedPubMedCentral Lee JS, Lee JH, Lee KE, Kim JH, Hong JM, Ra EK et al (2016) Genotype–phenotype analysis of von Hippel–Lindau syndrome in Korean families: HIFα bindingsite missense mutations elevate age–specific risk for CNS hemangioblastoma. BMC Med Genet 17(1):48CrossRefPubMedPubMedCentral
43.
go back to reference Igarashi H, Ito T, Nishimori I et al (2014) Pancreatic involvement in Japanese patients with von Hippel–Lindau disease: results of a nationwide survey. J Gastroenterol 49(3):511–516CrossRefPubMed Igarashi H, Ito T, Nishimori I et al (2014) Pancreatic involvement in Japanese patients with von Hippel–Lindau disease: results of a nationwide survey. J Gastroenterol 49(3):511–516CrossRefPubMed
44.
go back to reference Binkovitz LA, Johnson CD, Stephens DH (1990) Islet cell tumors in von Hippel–Lindau disease: increased prevalence and relationship to the multiple endocrine neoplasias. AJR Am J Roentgenol 155(3):501–505CrossRefPubMed Binkovitz LA, Johnson CD, Stephens DH (1990) Islet cell tumors in von Hippel–Lindau disease: increased prevalence and relationship to the multiple endocrine neoplasias. AJR Am J Roentgenol 155(3):501–505CrossRefPubMed
45.
go back to reference Charlesworth M, Verbeke CS, Falk GA et al (2012) Pancreatic lesions in von Hippel–Lindau disease? A systematic review and meta–synthesis of the literature. J Gastrointest Surg 16(7):1422–1428CrossRefPubMed Charlesworth M, Verbeke CS, Falk GA et al (2012) Pancreatic lesions in von Hippel–Lindau disease? A systematic review and meta–synthesis of the literature. J Gastrointest Surg 16(7):1422–1428CrossRefPubMed
46.
go back to reference Blansfield JA, Choyke L, Morita SY, Choyke PL, Pingpank JF et al (2007) Clinical, genetic and radiographic analysis of 108 patients with von Hippel–Lindau disease (VHL) manifested by pancreatic neuroendocrine neoplasms (PNETs). Surgery 142(6):814–818CrossRefPubMed Blansfield JA, Choyke L, Morita SY, Choyke PL, Pingpank JF et al (2007) Clinical, genetic and radiographic analysis of 108 patients with von Hippel–Lindau disease (VHL) manifested by pancreatic neuroendocrine neoplasms (PNETs). Surgery 142(6):814–818CrossRefPubMed
47.
go back to reference Richards FM, Payne SJ, Zbar B, Affara NA et al (1995) Molecular analysis of de novo germline mutations in the von Hippel–Lindau disease gene. Hum Mol Genet 4(11):2139–2143CrossRefPubMed Richards FM, Payne SJ, Zbar B, Affara NA et al (1995) Molecular analysis of de novo germline mutations in the von Hippel–Lindau disease gene. Hum Mol Genet 4(11):2139–2143CrossRefPubMed
48.
go back to reference Oberlé I, Rousseau F, Heitz D, Kretz C, Devys D et al (1991) Instability of a 550 bp DNA segment and abnormal methylation in fragile X syndrome. Science 252(5009):1097–1102CrossRefPubMed Oberlé I, Rousseau F, Heitz D, Kretz C, Devys D et al (1991) Instability of a 550 bp DNA segment and abnormal methylation in fragile X syndrome. Science 252(5009):1097–1102CrossRefPubMed
49.
go back to reference La Spada AR, Wilson EM, Lubahn DB et al (1991) Androgen receptor gene mutations in X–linked spinal and bulbar muscular atrophy. Nature 352(6330):77–79CrossRefPubMed La Spada AR, Wilson EM, Lubahn DB et al (1991) Androgen receptor gene mutations in X–linked spinal and bulbar muscular atrophy. Nature 352(6330):77–79CrossRefPubMed
50.
go back to reference Mahadevan M, Tsilfidis C, Sabourin L, Shutler G et al (1992) Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene. Science 255(5049):1253–1255CrossRefPubMed Mahadevan M, Tsilfidis C, Sabourin L, Shutler G et al (1992) Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene. Science 255(5049):1253–1255CrossRefPubMed
51.
go back to reference Ranen NG, Stine OC, Abbott MH et al (1995) Anticipation and instability of IT–15 (CAG)n repeats in parent–offspring pairs with Huntington disease. Am J Hum Genet 57(3):593–602PubMedPubMedCentral Ranen NG, Stine OC, Abbott MH et al (1995) Anticipation and instability of IT–15 (CAG)n repeats in parent–offspring pairs with Huntington disease. Am J Hum Genet 57(3):593–602PubMedPubMedCentral
52.
go back to reference Tabori U, Nanda S, Druker H, Lees J, Malkin D (2007) Younger age of cancer initiation is associated with shorter telomere length in Li–Fraumeni syndrome. Cancer Res 67(4):1415–1418CrossRefPubMed Tabori U, Nanda S, Druker H, Lees J, Malkin D (2007) Younger age of cancer initiation is associated with shorter telomere length in Li–Fraumeni syndrome. Cancer Res 67(4):1415–1418CrossRefPubMed
53.
go back to reference Martinez–Delgado B, Yanowsky K, Inglada–Perez L et al (2011) Genetic anticipation is associated with telomere shortening in hereditary breast cancer. PLoS Genet 7(7):e1002182CrossRefPubMedPubMedCentral Martinez–Delgado B, Yanowsky K, Inglada–Perez L et al (2011) Genetic anticipation is associated with telomere shortening in hereditary breast cancer. PLoS Genet 7(7):e1002182CrossRefPubMedPubMedCentral
54.
55.
go back to reference Nilbert M, Timshel S, Bernstein I, Larsen K (2009) Role for genetic anticipation in Lynch syndrome. J Clin Oncol 27(3):360–364CrossRefPubMed Nilbert M, Timshel S, Bernstein I, Larsen K (2009) Role for genetic anticipation in Lynch syndrome. J Clin Oncol 27(3):360–364CrossRefPubMed
Metadata
Title
Genotype phenotype correlation in Asian Indian von Hippel–Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma
Authors
Nilesh Lomte
Sanjeet Kumar
Vijaya Sarathi
Reshma Pandit
Manjunath Goroshi
Swati Jadhav
Anurag R. Lila
Tushar Bandgar
Nalini S. Shah
Publication date
01-07-2018
Publisher
Springer Netherlands
Published in
Familial Cancer / Issue 3/2018
Print ISSN: 1389-9600
Electronic ISSN: 1573-7292
DOI
https://doi.org/10.1007/s10689-017-0058-y

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