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Genetic association studies of cleft lip andlor palate with hypodontia outside the cleft regionSLAYTON, Rebecca L; WILLIAMS, Laura; MURRAY, Jeffrey C et al.The Cleft palate-craniofacial journal. 2003, Vol 40, Num 3, pp 274-279, issn 1055-6656, 6 p.Article

Recurrent Atypical Hemolytic Uremic Syndrome Associated With Factor I Mutation in a Living Related Renal Transplant RecipientCHAN, Micah R; THOMAS, Christie P; TORREALBA, Jose R et al.American journal of kidney diseases. 2009, Vol 53, Num 2, pp 321-326, issn 0272-6386, 6 p.Article

Genotype-phenotype correlations for SLC26A4-related deafnessAZAIEZ, Hela; TAO YANG; PRASAD, Sai et al.Human genetics. 2007, Vol 122, Num 5, pp 451-457, issn 0340-6717, 7 p.Article

A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndromeMAGA, Tara K; MEYER, Nicole C; BELSHA, Craig et al.Nephrology, dialysis, transplantation (Print). 2011, Vol 26, Num 2, pp 739-741, issn 0931-0509, 3 p.Article

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier geneHILGERT, Nele; HUENTELMAN, Matthew J; CASTORINA, Pierangela et al.European journal of human genetics. 2009, Vol 17, Num 4, pp 517-524, issn 1018-4813, 8 p.Article

Identification of three novel TECTA mutations in iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locusMEYER, Nicole C; ALASTI, Fatemeh; SMITH, Richard J. H et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 14, pp 1623-1629, issn 1552-4825, 7 p.Article

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