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Faiyaz-ul-Haque, M.
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1

Vitamin D Receptor FokI, ApaI, and TaqI Polymorphisms in Le..:

Shaik, Abjal Pasha ; Alsaeed, Abbas H. ; Faiyaz-ul-Haque, M....
Frontiers in Genetics.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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2

A novel missense mutation in theHAX1gene in severe congenit..:

Faiyaz-Ul-Haque, M ; Al-Jefri, A ; Abalkhail, HA...
Clinical Genetics.  76 (2009)  6 - p. 569-572 , 2009
Link: https://doi.org/10.1111/..
 
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3

A family exhibiting arterial tortuosity syndrome displays h..:

Zaidi, SHE ; Peltekova, V ; Meyer, S...
Clinical Genetics.  67 (2004)  2 - p. 183-188 , 2004
Link: https://doi.org/10.1111/..
 
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4

Fine mapping of the X-linked split-hand/split-foot malforma..:

Faiyaz-Ul-Haque, M ; Zaidi, SHE ; King, LM...
Clinical Genetics.  67 (2004)  1 - p. 93-97 , 2004
Link: https://doi.org/10.1111/..
 
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5

A novel HAX1 gene mutation in severe congenital neutropenia..:

Faiyaz-Ul-Haque, Muhammad ; Al-Jefri, Abdullah ; Al-Dayel, Fouad...
European Journal of Pediatrics.  169 (2010)  6 - p. 661-666 , 2010
Link: https://doi.org/10.1007/..
 
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6

Alopecia Universalis Associated with a Mutation in the Huma..:

Ahmad, Wasim ; Muhammad Faiyaz ul Haque ; Brancolini, Valeria...
Science.  279 (1998)  5351 - p. 720-724 , 1998
Link: https://www.jstor.org/st..
 
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7

Table_1_Vitamin D Receptor FokI, ApaI, and TaqI Polymorphis..:

Abjal Pasha Shaik ; Abbas H. Alsaeed ; M. Faiyaz-ul-Haque...
doi:10.3389/fgene.2019.00388.s001.  , 2019
Link: https://doi.org/10.3389/..
 
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8

Vitamin D Receptor FokI, ApaI, and TaqI Polymorphisms in Le..:

Abjal Pasha Shaik ; Abbas H. Alsaeed ; M. Faiyaz-ul-Haque...
https://www.frontiersin.org/article/10.3389/fgene.2019.00388/full.  , 2019
Link: https://doi.org/10.3389/..
 
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9

A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Th..:

Rafiq, Muhammad Arshad ; Ansar, Muhammad ; Mahmood, Saqib...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157275/.  , 2004
Link: http://www.ncbi.nlm.nih...
 
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10

A locus for hereditary hypotrichosis localized to human chr..:

Rafique, Muhammad Arshad ; Ansar, Muhammad ; Jamal, Syed Muhammad...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157268/.  , 2003
Link: http://www.ncbi.nlm.nih...
 
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11

A novel autosomal recessive non-syndromic deafness locus (D..:

Ansar, Muhammad ; Din, Mohammad Amin ud ; Arshad, Muhammad...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2917542.  , 2003
Link: http://www.ncbi.nlm.nih...
 
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12

Alopecia Universalis Associated with a Mutation in the Huma..:

Ahmad, Wasim ; Faiyaz ul Haque, Muhammad ; Brancolini, Valeria...
Science.  279 (1998)  5351 - p. 720-724 , 1998
Link: https://doi.org/10.1126/..
 
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13

A Locus for Autosomal Recessive Hypodontia with Associated ..:

Ahmad, Wasim ; Brancolini, Valeria ; Faiyaz ul Haque, Muhammad...
The American Journal of Human Genetics.  62 (1998)  4 - p. 987-991 , 1998
Link: https://doi.org/10.1086/..
 
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14

A gene for universal congenital alopecia maps to chromosome..:

Nöthen, M M ; Cichon, S ; Vogt, I R...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1376893.  , 1998
Link: http://www.ncbi.nlm.nih...
 
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15

Mutations in orthologous genes in human spondyloepimetaphys..:

Haque, Muhammad Faiyaz ul ; King, Lily M. ; Krakow, Deborah...
Nature Genetics.  20 (1998)  2 - p. 157-162 , 1998
Link: https://doi.org/10.1038/..
 
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