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Human Molecular Genetics|May 16, 1998
Non-disjunction of chromosome 18M Bugge, A Collins, M B Petersen, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Human Mutation|March 3, 1998
Constant denaturant gel electrophoresis (CDGE) in BRCA1 mutation screeningT I Andersen, H G Eiken, F Couch, et al.
Cardiovascular Diabetology|May 13, 2023
Diabetes is accompanied by secretion of pro-atherosclerotic exosomes from vascular smooth muscle cellsHeng Yu, Hunter F Douglas, Donald Wathieu, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldA Lund, B Udd, V Juvonen, et al.
American Journal of Human Genetics|May 12, 2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, G E Tiller, M Le Merrer, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidismB T Teh, S Kytölä, F Farnebo, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
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