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Human Genetics|December 1, 1988
Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosomeS Szpiro-Tapia, A Sefiani, M Guilloud-Bataille, et al.European Journal of Medical Genetics|May 23, 2020
Exome sequencing revealed a novel homozygous METTL23 gene mutation leading to familial mild intellectual disability with dysmorphic featuresW Smaili, S Chafai Elalaoui, A Zrhidri, et al.International Journal of Legal Medicine|February 24, 2001
Y chromosome STR haplotypes in four populations from northwest AfricaE Bosch, F Calafell, A Pérez-Lezaun, et al.Balkan Journal of Medical Genetics : BJMG|March 14, 2024
Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case ReportA Lamzouri, A El Rherbi, I Ratbi, et al.Journal of Medical Genetics|April 1, 1994
Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.Human Genetics|January 1, 1991
Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markersA Sefiani, R M'rad, L Simard, et al.Human Genetics|November 1, 1988
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11A Sefiani, D Sinnett, L Abel, et al.Annales De Genetique|January 1, 1989
The anonymous PAS45 probe detects RFLPs in 13q31M S Gross, A Sefiani, M F de Tand, et al.Human Mutation|March 14, 2007
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locusE Bal, L Baala, C Cluzeau, et al.Clinical Genetics|September 10, 2010
Molecular analysis of Sanfilippo syndrome type C in Spain: seven novel HGSNAT mutations and characterization of the mutant allelesI Canals, S C Elalaoui, M Pineda, et al.Pageof 5