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'All is done by Allah'. Understandings of Down syndrome and prenatal testing in PakistanBRYANT, Louise D; AHMED, Shenaz; AHMED, Mushtaq et al.Social science & medicine (1982). 2011, Vol 72, Num 8, pp 1393-1399, issn 0277-9536, 7 p.Article

Genotype-Phenotype Correlation for Leber Congenital Amaurosis in Northern PakistanMCKIBBIN, Martin; ALI, Manir; MOHAMED, Moin D et al.Archives of ophthalmology (1960). 2010, Vol 128, Num 1, pp 107-113, issn 0003-9950, 7 p.Article

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defectsKHAN, Kamron; LOGAN, Clare V; POULTER, James A et al.Human molecular genetics (Print). 2012, Vol 21, Num 4, pp 776-783, issn 0964-6906, 8 p.Article

Null Mutations in LTBP2 Cause Primary Congenital GlaucomaALI, Manir; MCKIBBIN, Martin; GILMOUR, David F et al.American journal of human genetics. 2009, Vol 84, Num 5, pp 664-671, issn 0002-9297, 8 p.Article

Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental GlaucomaKHAN, Kamron; RUDKIN, Adam; SHIRES, Mike et al.American journal of human genetics. 2011, Vol 89, Num 3, pp 464-473, issn 0002-9297, 10 p.Article

An SCN9A channelopathy causes congenital inability to experience painCOX, James J; REIMANN, Frank; AL-GAZALI, Lihadh et al.Nature (London). 2006, Vol 444, Num 7121, pp 894-898, issn 0028-0836, 5 p.Article

Umbilical vein oxytocin for the treatment of retained placenta (Release Study): a double-blind, randomised controlled trialWEEKS, Andrew D; ALIA, Godfrey; FAIRLIE, Fiona et al.Lancet (British edition). 2010, Vol 375, Num 9709, pp 141-147, issn 0140-6736, 7 p.Article

Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genesMICHIELSE, Caroline B; BHAT, Meena; BRADY, Angela et al.European journal of human genetics. 2006, Vol 14, Num 12, pp 1306-1312, issn 1018-4813, 7 p.Article

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