M. Amin-ud-din

发表

Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene

M. Rafiq, P. John, W. Ahmad, 2005, Archives of Dermatological Research.

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

W. Ahmad, M. Amin-ud-din, M. Jelani, 2008, Human Genetics.

DDT residue and its metabolites in dried fishes of Dhaka city markets

M. Amin-ud-din, M. Chowdhury, M. Malek, 2010 .

Mutation of ATF6 causes autosomal recessive achromatopsia

J. Shendure, D. Nickerson, S. Leal, 2015, Human Genetics.

A nonsense mutation in the gene ROR2 underlying autosomal dominant brachydactyly type B

W. Ahmad, R. Habib, M. Amin-ud-din, 2013, Clinical dysmorphology.

EFFECTS OF ANIMAL MANURE ON THE GROWTH AND DEVELOPMENT OF OKRA (Abelmoschus esculentus L.)

M. Amin-ud-din, D. G. Khan, H. M. Saeed, 2013 .

Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1‐17q25.3

W. Ahmad, M. Amin-ud-din, S. Haque, 2004, Clinical genetics.

Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish.

J. Shendure, D. Nickerson, S. Leal, 2014, Human molecular genetics.

Mapping of three novel loci for non‐syndromic autosomal recessive mental retardation (NS‐ARMR) in consanguineous families from Pakistan

L. Feuk, A. Noor, M. Amin-ud-din, 2010, Clinical genetics.

Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability

J. Vincent, M. Rafiq, Farooq Naeem, 2016, Journal of Human Genetics.

Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins

I. Waheed, P. John, W. Ahmad, 2006, Archives of Dermatological Research.

Genetic heterogeneity and gene diversity at ABO and Rh loci in the human population of Southern Punjab, Pakistan.

M. Amin-ud-din, S. Malik, 2013 .

Distribution of ABO and Rh D blood groups in the population of Poonch District, Azad Jammu and Kashmir.

M. Amin-ud-din, M. Khan, M. Akhtar, 2009, Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit.

Studies on shape, size and weight of certain weed seeds buried in the soil seed bank.

M. Akhtar, A. Bakhsh, M. Amin-ud-din, 2006 .

Mutation of ATF6 causes autosomal recessive achromatopsia

J. Shendure, D. Nickerson, S. Leal, 2015, Human Genetics.

A novel type of autosomal recessive syndactyly: Clinical and molecular studies in a family of Pakistani origin

K. Grzeschik, M. Koch, W. Ahmad, 2004, American journal of medical genetics. Part A.

Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21.31

K. Grzeschik, M. Koch, W. Ahmad, 2005, European Journal of Human Genetics.

Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features

J. Vincent, M. Rafiq, L. Mottron, 2015, BMC Medical Genetics.

Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.

A. Ballabio, M. Rafiq, P. Aridon, 2001, American journal of medical genetics.