Dermatology

A comprehensive association analysis confirms ZMIZ1 to be a susceptibility gene for vitiligo in Chinese population
Yonghu Sun, Xianbo Zuo, Xiaodong Zheng, Fusheng Zhou, Bo Liang, Hong Liu, Ruixue Chang, Jinping Gao, Yujun Sheng, Hongzhou Cui, Wenjun Wang, Anand Kumar Andiappan, Olaf Rotzschke, Sen Yang, Liangdan Sun, Furen Zhang, Xuejun Zhang, Yunqing Ren, Jianjun Liu

Journal of Medical Genetics May 2014, 51 (5) 345-353; DOI: 10.1136/jmedgenet-2013-102233
Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion
Isabelle Coupry, Laurence Taine, Cyril Goizet, Carine Soriano, Bruno Mortemousque, Benoît Arveiler, Didier Lacombe

Journal of Medical Genetics Jan 2001, 38 (1) 35-38; DOI: 10.1136/jmg.38.1.35
Epigenetic inheritance of telomere length obscures identification of causative PARN locus
Chao Xing, Christine Kim Garcia

Journal of Medical Genetics May 2016, 53 (5) 356-358; DOI: 10.1136/jmedgenet-2015-103685
LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome
Caroline Gaudy-Marqueste, Patrice Roll, Vera Esteves-Vieira, Pierre-Jean Weiller, Jean Jacques Grob, Pierre Cau, Nicolas Lévy, Annachiara De Sandre-Giovannoli

Journal of Medical Genetics Jun 2010, 47 (6) 361-370; DOI: 10.1136/jmg.2009.071696
X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11
Petter Strømme, Kjetil Sundet, Cato Mørk, Jean-Jacques Cassiman, Jean-Pierre Fryns, Stephan Claes

Journal of Medical Genetics May 1999, 36 (5) 374-378; DOI: 10.1136/jmg.36.5.374
The p63 gene in EEC and other syndromes
H G Brunner, B C J Hamel, H van Bokhoven

Journal of Medical Genetics Jun 2002, 39 (6) 377-381; DOI: 10.1136/jmg.39.6.377
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair
Yuval Ramot, Vered Molho-Pessach, Tomer Meir, Ruslana Alper-Pinus, Ihab Siam, Spiro Tams, Sofia Babay, Abraham Zlotogorski

Journal of Medical Genetics Jun 2014, 51 (6) 388-394; DOI: 10.1136/jmedgenet-2014-102346
Comprehensive analysis of CDKN2A (p16^INK4A/p14^ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma
K Laud, C Marian, M F Avril, M Barrois, A Chompret, A M Goldstein, M A Tucker, P A Clark, G Peters, V Chaudru, F Demenais, A Spatz, M W Smith, G M Lenoir, B Bressac-de Paillerets

Journal of Medical Genetics Jan 2006, 43 (1) 39-47; DOI: 10.1136/jmg.2005.033498
Recessive primary congenital lymphoedema caused by a VEGFR3 mutation
A Ghalamkarpour, W Holnthoner, P Saharinen, L M Boon, J B Mulliken, K Alitalo, M Vikkula

Journal of Medical Genetics Jun 2009, 46 (6) 399-404; DOI: 10.1136/jmg.2008.064469
Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy
D Araújo-Vilar, G Lattanzi, B González-Méndez, A T Costa-Freitas, D Prieto, M Columbaro, E Mattioli, B Victoria, N Martínez-Sánchez, A Ramazanova, M Fraga, A Beiras, J Forteza, L Domínguez-Gerpe, C Calvo, J Lado-Abeal

Journal of Medical Genetics Jan 2009, 46 (1) 40-48; DOI: 10.1136/jmg.2008.059485

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