Muhammad Faiyaz‐Ul‐Haque

Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers–Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (β4GalT-7)

Daniela G. Seidler, Muhammad Faiyaz‐Ul‐Haque, Uwe Hansen et al. · Journal of Molecular Medicine · 2006 · 114 citations

Autoimmune Disease, Cutaneous Biology, Defective Glycosylation +8

A novel missense mutation in the galactosyltransferase‐I (<i>B4GALT7</i>) gene in a family exhibiting facioskeletal anomalies and Ehlers–Danlos syndrome resembling the progeroid type

Muhammad Faiyaz‐Ul‐Haque, Syed Hassan Ejaz Zaidi, Mariam Al‐Ali et al. · American Journal of Medical Genetics Part A · 2004 · 108 citations

Mutation in the cartilage‐derived morphogenetic protein‐1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)

Muhammad Faiyaz‐Ul‐Haque, Wasim Ahmad, SHE Zaidi et al. · Clinical Genetics · 2002 · 86 citations

Novel mutation in the gene encoding c‐Abl‐binding protein SH3BP2 causes cherubism

Muhammad Faiyaz‐Ul‐Haque, Shelley Kennedy, Richard I. Aviv et al. · American Journal of Medical Genetics Part A · 2003 · 58 citations

Fine mapping of the X‐linked split‐hand/split‐foot malformation (SHFM2) locus to a 5.1‐Mb region on Xq26.3 and analysis of candidate genes

Muhammad Faiyaz‐Ul‐Haque, SHE Zaidi, LM King et al. · Clinical Genetics · 2004 · 54 citations