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Center director:
Prof. Niels Tommerup
tommerup@imbg.ku.dk







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Muhammad Farooq

Ph.d. student / Ph.d. studerende

Autosomal recessive microcephaly in inbred Pakistani families

Emailfarooq_nibge@yahoo.com

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Search PubMed for articles by Muhammad Farooq

Publications related to WJC

3.   Hussain MS, Bakhtiar SM, Farooq M, Anjum I, Janzen E, Toliat MR, Eiberg H, Kjaer KW, Tommerup N, Noegel AA, Nürnberg P, Baig SM, Hansen L. Genetic heterogeneity in Pakistani microcephaly families. Clin Genet. 2012 Jul 6;9999(999A). doi: 10.1111/j.1399-0004.2012.01932.x. [Epub ahead of print].
 
2.   Farooq M, Baig S, Tommerup N, Kjaer KW. Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1. Am J Med Genet A. 2010;152A:495-7.
 
1.   Farooq M, Troelsen JT, Boyd M, Eiberg H, Hansen L, Hussain MS, Rehman SU, Azhar A, Ali A, Bakhtiar SM, Tommerup N, Baig SM, Kjaer KW. Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS. Eur J Hum Genet. 2010;18:733-6.
 

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