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American Journal of Medical Genetics|October 15, 1994
Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindredE Dow, S Cross, D J Wolgemuth, et al.Journal of Medical Genetics|March 10, 2001
MECP2 mutation in non-fatal, non-progressive encephalopathy in a maleB Imessaoudene, J P Bonnefont, G Royer, et al.European Journal of Biochemistry|April 15, 1989
Apolipoprotein-E-gene expression in rat liver during development in relation to insulin and glucagonM Mangeney, P Cardot, S Lyonnet, et al.Annales De Dermatologie Et De Venereologie|June 23, 2012
[Clinical features of Spitz naevus in children: a retrospective study of 196 cases]L Le Saché-de Peufeilhoux, I Moulonguet, B Cavelier-Balloy, et al.American Journal of Medical Genetics|March 17, 1997
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeV Cormier-Daire, M Le Merrer, N Gigarel, et al.Human Genetics|November 1, 1994
A novel polymorphism in the coding sequence of the human RET proto-oncogeneP Edery, T Attié, L M Mulligan, et al.Heart (British Cardiac Society)|April 16, 1998
Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defectM Chessa, G Butera, P Bonhoeffer, et al.Prenatal Diagnosis|June 1, 1993
Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markersF Serville, P Benit, P Saugier, et al.Journal of Medical Genetics|April 16, 1999
Investigation of germline GFR alpha-1 mutations in Hirschsprung diseaseS M Myers, R Salomon, A Goessling, et al.European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.Pageof 38