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L Al-Gazali

Showing results (11-20 of 26) with videos related to

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Community Genetics|March 16, 2005
Genetic contribution to high neonatally lethal malformation rate in the United Arab EmiratesA Dawodu, L Al-Gazali, E Varady, et al.
Journal of Medical Genetics|January 1, 1994
The spectrum of beta thalassaemia mutations in the UAE national populationR Quaife, L al-Gazali, S Abbes, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 22, 2011
Stuve-Wiedemann syndrome: a skeletal dysplasia characterized by bowed long bonesM A Begam, W Alsafi, G N Bekdache, et al.
American Journal of Human Genetics|December 1, 1999
Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneityK Saar, L Al-Gazali, L Sztriha, et al.
Clinical Genetics|February 15, 2018
A B3GALT6 variant in patient originally described as Al-Gazali syndrome and implicating the endoplasmic reticulum quality control in the mechanism of some β3GalT6-pathy mutationsA Ben-Mahmoud, S Ben-Salem, M Al-Sorkhy, et al.
Journal of Medical Genetics|April 5, 2003
Diagnostic criteria, clinical characteristics, and natural history of Cohen syndromeK E Chandler, A Kidd, L Al-Gazali, et al.
Journal of Medical Genetics|September 3, 2002
Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate geneS Eyre, P Roby, K Wolstencroft, et al.
Chromosoma|August 20, 1997
Centromeric inactivation in a dicentric human Y;21 translocation chromosomeA M Fisher, L Al-Gazali, T Pramathan, et al.
Human Genetics|July 11, 2002
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patientsA M Slavotinek, C Searby, L Al-Gazali, et al.
Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Community Genetics|March 16, 2005
Genetic contribution to high neonatally lethal malformation rate in the United Arab EmiratesA Dawodu, L Al-Gazali, E Varady, et al.
Journal of Medical Genetics|January 1, 1994
The spectrum of beta thalassaemia mutations in the UAE national populationR Quaife, L al-Gazali, S Abbes, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 22, 2011
Stuve-Wiedemann syndrome: a skeletal dysplasia characterized by bowed long bonesM A Begam, W Alsafi, G N Bekdache, et al.
American Journal of Human Genetics|December 1, 1999
Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneityK Saar, L Al-Gazali, L Sztriha, et al.
Clinical Genetics|February 15, 2018
A B3GALT6 variant in patient originally described as Al-Gazali syndrome and implicating the endoplasmic reticulum quality control in the mechanism of some β3GalT6-pathy mutationsA Ben-Mahmoud, S Ben-Salem, M Al-Sorkhy, et al.
Journal of Medical Genetics|April 5, 2003
Diagnostic criteria, clinical characteristics, and natural history of Cohen syndromeK E Chandler, A Kidd, L Al-Gazali, et al.
Journal of Medical Genetics|September 3, 2002
Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate geneS Eyre, P Roby, K Wolstencroft, et al.
Chromosoma|August 20, 1997
Centromeric inactivation in a dicentric human Y;21 translocation chromosomeA M Fisher, L Al-Gazali, T Pramathan, et al.
Human Genetics|July 11, 2002
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patientsA M Slavotinek, C Searby, L Al-Gazali, et al.
Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Pageof 3