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Clinical Genetics
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February 4, 2012
Stüve-Wiedemann syndrome and related bent bone dysplasias
N A Akawi, B R Ali, L Al-Gazali
Clinical Genetics
|
June 15, 2011
Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations
N A Akawi, L Al-Gazali, B R Ali
Australasian Radiology
|
May 17, 2007
Radiological manifestations of the skeleton, lungs and brain in Stueve-Wiedemann syndrome
R Langer, L Al-Gazali, P Raupp, et al.
Journal of Medical Genetics
|
August 28, 1999
A syndrome of immune complex glomerulonephritis and ophthalmic abnormalities
I Amirlak, S G Sabnis, L Al-Gazali, et al.
Neurology
|
May 22, 1998
Agyria-pachygyria and agenesis of the corpus callosum: autosomal recessive inheritance with neonatal death
L Sztriha, L Al-Gazali, A Dawodu, et al.
Pediatric Neurology
|
May 20, 1998
Microlissencephaly
L Sztriha, L Al-Gazali, E Várady, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 8, 1998
Mental health problems among schoolchildren in United Arab Emirates: prevalence and risk factors
V Eapen, L al-Gazali, S Bin-Othman, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2008
A new autosomal recessive syndrome of ocular colobomas, ichthyosis, brain malformations and endocrine abnormalities in an inbred Emirati family
L Al-Gazali, J Hertecant, K Algawi, et al.
Molecular Syndromology
|
April 20, 2013
A Novel Aberrant Splice Site Mutation in RAB23 Leads to an Eight Nucleotide Deletion in the mRNA and Is Responsible for Carpenter Syndrome in a Consanguineous Emirati Family
S Ben-Salem, M A Begum, B R Ali, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
October 17, 2013
Fibrochondrogenesis: prenatal diagnosis and outcome
G N Bekdache, M A Begam, F Chedid, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 3
Clinical Genetics
|
February 4, 2012
Stüve-Wiedemann syndrome and related bent bone dysplasias
N A Akawi, B R Ali, L Al-Gazali
Clinical Genetics
|
June 15, 2011
Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations
N A Akawi, L Al-Gazali, B R Ali
Australasian Radiology
|
May 17, 2007
Radiological manifestations of the skeleton, lungs and brain in Stueve-Wiedemann syndrome
R Langer, L Al-Gazali, P Raupp, et al.
Journal of Medical Genetics
|
August 28, 1999
A syndrome of immune complex glomerulonephritis and ophthalmic abnormalities
I Amirlak, S G Sabnis, L Al-Gazali, et al.
Neurology
|
May 22, 1998
Agyria-pachygyria and agenesis of the corpus callosum: autosomal recessive inheritance with neonatal death
L Sztriha, L Al-Gazali, A Dawodu, et al.
Pediatric Neurology
|
May 20, 1998
Microlissencephaly
L Sztriha, L Al-Gazali, E Várady, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 8, 1998
Mental health problems among schoolchildren in United Arab Emirates: prevalence and risk factors
V Eapen, L al-Gazali, S Bin-Othman, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2008
A new autosomal recessive syndrome of ocular colobomas, ichthyosis, brain malformations and endocrine abnormalities in an inbred Emirati family
L Al-Gazali, J Hertecant, K Algawi, et al.
Molecular Syndromology
|
April 20, 2013
A Novel Aberrant Splice Site Mutation in RAB23 Leads to an Eight Nucleotide Deletion in the mRNA and Is Responsible for Carpenter Syndrome in a Consanguineous Emirati Family
S Ben-Salem, M A Begum, B R Ali, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
October 17, 2013
Fibrochondrogenesis: prenatal diagnosis and outcome
G N Bekdache, M A Begam, F Chedid, et al.
Page
of 3