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International Journal of Pediatric Otorhinolaryngology|September 1, 1986
Choanal atresia and deafnessA Robier, M J Ployet, B Loustalot, et al.American Journal of Medical Genetics|March 21, 1998
X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one familyM Raynaud, N Ronce, A D Ayrault, et al.American Journal of Medical Genetics|November 4, 1998
Are Dp71 and Dp140 brain dystrophin isoforms related to cognitive impairment in Duchenne muscular dystrophy?M P Moizard, C Billard, A Toutain, et al.American Journal of Medical Genetics|September 1, 1984
Opsismodysplasia: a new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebraeP Maroteaux, V Stanescu, R Stanescu, et al.European Journal of Human Genetics : EJHG|March 1, 1997
Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardationT Bienvenu, H Der-Sarkissian, P Billuart, et al.Annales De Genetique|January 1, 1984
[The r(14) syndrome. 3 new observations]S Gilgenkrantz, A Morali, M Vidailhet, et al.Annales De Pediatrie|January 1, 1991
[Reinhardt-Pfeiffer mesomelic dysplasia or dyschondrosteosis? Is the distinction well-founded? Apropos of a familial case with variable expression]A Toutain, D Sirinelli, C Paillet, et al.Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 1, 1996
Twenty-day cerebral and umbilical Doppler monitoring on a growth retarded and hypoxic fetusA Fignon, A Salihagic, S Akoka, et al.Therapie|September 1, 1994
[Pentasa (mesalazine) and pregnancy]A P Jonville-Bera, C Soyez, A Fignon, et al.Pageof 11