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M Faiyaz-Ul-Haque

Showing results (1-10 of 23) with videos related to

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Clinical Genetics|June 11, 2009
Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in the SLC2A10 geneS H E Zaidi, S Meyer, I Peltekova, et al.
American Journal of Medical Genetics. Part A|August 6, 2003
Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubismBryan Lo, M Faiyaz-Ul-Haque, S Kennedy, et al.
Human Genetics|March 1, 1993
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1M Faiyaz ul Haque, S Uhlhaas, M Knapp, et al.
Klinische Padiatrie|January 11, 2005
[Arterial tortuosity syndrome]S Meyer, M Faiyaz-Ul-Haque, M Zankl, et al.
Clinical Genetics|February 27, 2004
The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23B Lo, M Faiyaz-Ul-Haque, B Banwell, et al.
Clinical Genetics|July 31, 2007
Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from QatarM Faiyaz-Ul-Haque, S H E Zaidi, M S Al-Mureikhi, et al.
Frontiers in Genetics|May 14, 2019
Vitamin D Receptor <i>FokI, ApaI</i>, and <i>TaqI</i> Polymorphisms in Lead Exposed Subjects From Saudi ArabiaAbjal Pasha Shaik, Abbas H Alsaeed, M Faiyaz-Ul-Haque, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Clinical Genetics|February 1, 2005
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13S H E Zaidi, V Peltekova, S Meyer, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Clinical Genetics|June 11, 2009
Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in the SLC2A10 geneS H E Zaidi, S Meyer, I Peltekova, et al.
American Journal of Medical Genetics. Part A|August 6, 2003
Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubismBryan Lo, M Faiyaz-Ul-Haque, S Kennedy, et al.
Human Genetics|March 1, 1993
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1M Faiyaz ul Haque, S Uhlhaas, M Knapp, et al.
Klinische Padiatrie|January 11, 2005
[Arterial tortuosity syndrome]S Meyer, M Faiyaz-Ul-Haque, M Zankl, et al.
Clinical Genetics|February 27, 2004
The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23B Lo, M Faiyaz-Ul-Haque, B Banwell, et al.
Clinical Genetics|July 31, 2007
Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from QatarM Faiyaz-Ul-Haque, S H E Zaidi, M S Al-Mureikhi, et al.
Frontiers in Genetics|May 14, 2019
Vitamin D Receptor <i>FokI, ApaI</i>, and <i>TaqI</i> Polymorphisms in Lead Exposed Subjects From Saudi ArabiaAbjal Pasha Shaik, Abbas H Alsaeed, M Faiyaz-Ul-Haque, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Clinical Genetics|February 1, 2005
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13S H E Zaidi, V Peltekova, S Meyer, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Pageof 3