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American Journal of Medical Genetics|June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spotsH G Brunner, T Hulsebos, P M Steijlen, et al.The American Journal of Psychiatry|July 7, 2011
Association of the Alzheimer's gene SORL1 with hippocampal volume in young, healthy adultsJanita Bralten, Alejandro Arias-Vásquez, Remco Makkinje, et al.Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.Human Molecular Genetics|September 1, 1994
A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 geneH G Brunner, S E van Beersum, M L Warman, et al.American Journal of Medical Genetics|June 13, 1997
Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 geneM A van Steensel, P Buma, M C de Waal Malefijt, et al.Journal of Natural Products|April 1, 1997
The secalosides, novel tumor cell growth inhibitory glycosides from a pollen extractJ C Jaton, K Roulin, K Rose, et al.Clinical Dysmorphology|January 1, 1996
Ectrodactyly of lower limbs, congenital heart defect and characteristic facies in four unrelated Dutch patients: a new associationJ J Van Den Ende, C J Van Der Burgt, M C Jansweijer, et al.Molecular Endocrinology (Baltimore, Md.)|June 17, 1998
A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotypeJ W Martens, M Verhoef-Post, N Abelin, et al.The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
A missense mutation in the second transmembrane segment of the luteinizing hormone receptor causes familial male-limited precocious pubertyR Kraaij, M Post, H Kremer, et al.Journal of Hepatology|February 1, 1993
Serum bile acids and esterified bilirubin in early detection and differential diagnosis of hepatic dysfunction following orthotopic liver transplantationM Muraca, K Kohlhaw, M T Vilei, et al.Pageof 73