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Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Endocrine Reviews|October 26, 2010
Child health, developmental plasticity, and epigenetic programmingZ Hochberg, R Feil, M Constancia, et al.
Journal of Medical Genetics|July 22, 2005
Congenital hyperinsulinism and mosaic abnormalities of the ploidyI Giurgea, D Sanlaville, J-C Fournet, et al.
Nucleic Acids Research|February 21, 1998
Marfan Database (third edition): new mutations and new routines for the softwareG Collod-Béroud, C Béroud, L Ades, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Journal of Neurology|September 19, 2000
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophyH B Ginjaar, A J van der Kooi, H Ceelie, et al.
American Journal of Human Genetics|April 17, 1999
A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32M Varret, J P Rabès, B Saint-Jore, et al.
Journal of Dental Research|March 26, 2013
Common SNPs of AmelogeninX (AMELX) and dental caries susceptibilityB Gasse, S Grabar, A G Lafont, et al.
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