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The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.
Nat Genet. 2006 Feb;38(2):191-6. doi: 10.1038/ng1713. Epub 2006 Jan 15.
Nat Genet. 2006.
PMID: 16415887
Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies.
Szymanska K, Berry I, Logan CV, Cousins SR, Lindsay H, Jafri H, Raashid Y, Malik-Sharif S, Castle B, Ahmed M, Bennett C, Carlton R, Johnson CA.
Szymanska K, et al. Among authors: malik sharif s.
Cilia. 2012 Oct 1;1(1):18. doi: 10.1186/2046-2530-1-18.
Cilia. 2012.
PMID: 23351400
Free PMC article.
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Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.
Woods CG, Cox J, Springell K, Hampshire DJ, Mohamed MD, McKibbin M, Stern R, Raymond FL, Sandford R, Malik Sharif S, Karbani G, Ahmed M, Bond J, Clayton D, Inglehearn CF.
Woods CG, et al. Among authors: malik sharif s.
Am J Hum Genet. 2006 May;78(5):889-896. doi: 10.1086/503875. Epub 2006 Mar 21.
Am J Hum Genet. 2006.
PMID: 16642444
Free PMC article.
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Clinical features for diagnosis and management of patients with PRDM12 congenital insensitivity to pain.
Zhang S, Malik Sharif S, Chen YC, Valente EM, Ahmed M, Sheridan E, Bennett C, Woods G.
Zhang S, et al. Among authors: malik sharif s.
J Med Genet. 2016 Aug;53(8):533-5. doi: 10.1136/jmedgenet-2015-103646. Epub 2016 Mar 14.
J Med Genet. 2016.
PMID: 26975306
Free PMC article.
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