Sayedul Haque

Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse

Muhammad Faiyaz ul Haque, Lily King, Deborah Krakow et al. · Nature Genetics · 1998 · 211 citations

Biology, Developmental Biology, Somatic Variant +10

Cloning, Genomic Organization, Alternative Transcripts and Mutational Analysis of the Gene Responsible for Autosomal Recessive Universal Congenital Alopecia

Sven Cichon, M. Anker, Ina R. Vogt et al. · Human Molecular Genetics · 1998 · 153 citations

Biology, Developmental Biology, Mutational Analysis +15

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

A Gene for Universal Congenital Alopecia Maps to Chromosome 8p21-22

Markus M. Nöthen, Sven Cichon, Ina R. Vogt et al. · The American Journal of Human Genetics · 1998 · 62 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +5

Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindred

Mahmud Ahmad, Muhammad Faiyaz Ul Haque, Wasim Ahmad et al. · American Journal of Medical Genetics · 1998 · 61 citations