Drugs: endocrine system

Germline mutation analysis of the transforming growth factor β receptor type II (TGFBR2) and E-cadherin (CDH1) genes in early onset and familial colorectal cancer
LOVEENA VERMA, TIMOTHY R PORTER, FRANCES M RICHARDS, M HELEN RAJPAR, D GARETH R EVANS, FIONA MACDONALD, EAMONN R MAHER

Journal of Medical Genetics Feb 2001, 38 (2) e7; DOI: 10.1136/jmg.38.2.e7
Is growth hormone treatment beneficial or harmful in Costello syndrome?
B Kerr, M A Einaudi, P Clayton, G Gladman, T Eden, P Saunier, D Genevieve, N Philip

Journal of Medical Genetics Jun 2003, 40 (6) e74; DOI: 10.1136/jmg.40.6.e74
Alström syndrome: confirmation of linkage to chromosome 2p12-13 and phenotypic heterogeneity in three affected sibs
URS ZUMSTEG, PATRICK Y MULLER, ANDRÉ R MISEREZ

Journal of Medical Genetics Jul 2000, 37 (7) e8; DOI: 10.1136/jmg.37.7.e8
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss
Ghulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, Robert J Morell, Thomas B Friedman, Sadaf Naz

Journal of Medical Genetics Aug 2015, 52 (8) 548-552; DOI: 10.1136/jmedgenet-2015-103023
NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage
Christiane Messaed, Wafaa Chebaro, Raphael B Di Roberto, Cecile Rittore, Annie Cheung, Jocelyne Arseneau, Ariel Schneider, Moy Fong Chen, Kurt Bernishke, Urvashi Surti, Lori Hoffner, Philippe Sauthier, William Buckett, JianHua Qian, Nga Man Lau, Rashmi Bagga, James C Engert, Philippe Coullin, Isabelle Touitou, Rima Slim, H M Collaborative Group

Journal of Medical Genetics Aug 2011, 48 (8) 540-548; DOI: 10.1136/jmg.2011.089144
Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia
B Pérez, F Mechinaud, C Galambrun, N Ben Romdhane, B Isidor, N Philip, J Derain-Court, B Cassinat, J Lachenaud, S Kaltenbach, A Salmon, C Désirée, S Pereira, M L Menot, N Royer, O Fenneteau, A Baruchel, C Chomienne, A Verloes, H Cavé

Journal of Medical Genetics Oct 2010, 47 (10) 686-691; DOI: 10.1136/jmg.2010.076836
A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5
S G Cole, M E Begbie, G M F Wallace, C L Shovlin

Journal of Medical Genetics Jul 2005, 42 (7) 577-582; DOI: 10.1136/jmg.2004.028712

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