Showing results (2081-2090 of 9,576) with videos related to
Sort By:
Pageof 958
Human Genetics|December 17, 2013
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsisWilla Thorson, Oscar Diaz-Horta, Joseph Foster, et al.Human Genetics|February 1, 1987
Assignment of the myelin basic protein gene to human chromosome 18q22-qterR S Sparkes, T Mohandas, C Heinzmann, et al.Human Genetics|November 21, 2013
Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populationsShaolin Wang, Andrew D van der Vaart, Qing Xu, et al.Human Genetics|May 26, 2018
De novo FBXO11 mutations are associated with intellectual disability and behavioural anomaliesDaniel Fritzen, Alma Kuechler, Mona Grimmel, et al.Human Genetics|December 1, 1988
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumoursM Mannens, R M Slater, C Heyting, et al.Human Genetics|August 1, 1988
A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosomeS Y Li, C C Tsai, M Y Chou, et al.Human Genetics|January 1, 1979
Hurler-Scheie phenotype: a report of two pairs of inbred sibsN Kaibara, M Eguchi, K Shibata, et al.Human Genetics|January 1, 1994
Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nucleiD Cherif, H Der-Sarkissian, R BergerHuman Genetics|January 1, 1994
A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1-->q11.1A Kurimasa, Y Nagata, M Shimizu, et al.Human Genetics|January 1, 1994
Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresisX F Gu, F de Rooij, G Voortman, et al.Pageof 958