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Annales De Genetique|May 26, 1998
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11S C Deqaqi, M N'Guessan, J Forner, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Type 2 neurofibromatosis: intergenerational differences in genetic and clinical expression]A Drouet, F Le Moigne, D Salamé, et al.American Journal of Medical Genetics|May 8, 2000
X-linked congenital ataxia: a clinical and genetic studyE Bertini, V des Portes, G Zanni, et al.American Journal of Medical Genetics|July 9, 1999
Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)L B Jemaa, V des Portes, R Zemni, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 24, 2008
Abnormal Sylvian fissure on prenatal cerebral imaging: significance and correlation with neuropathological and postnatal dataL Guibaud, L Selleret, J C Larroche, et al.Human Molecular Genetics|April 20, 2001
MECP2 is highly mutated in X-linked mental retardationP Couvert, T Bienvenu, C Aquaviva, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1978
[Hemifacial microsomia and cardiac malformations. Apropos of 2 cases]P Morand, A Chantepie, C MorainePrenatal Diagnosis|May 29, 1998
High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocationA Guichet, S Briault, C MoraineRevue Francaise De Gynecologie Et D'Obstetrique|July 1, 1990
[What place is given to autopsy in cases of perinatal death?]C Berger, F Pierre, C MoraineSeizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.Pageof 11