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Human genetics

Showing results (871-880 of 9,569) with videos related to

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Human Genetics|October 1, 1995
Detection of a C-insertion polymorphism within the human tumor necrosis factor alpha (TNFA) geneB M Brinkman, E L Kaijzel, T W Huizinga, et al.
Human Genetics|October 1, 1995
An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndromeN G Pasteris, J L Gorski
Human Genetics|October 1, 1995
Dinucleotide repeat polymorphism at the D5S99 locus on chromosome 5q33-34I M Groenewald, L Warnich, A E Retief
Human Genetics|April 1, 1997
Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophyE Kondo-Iida, K Saito, H Tanaka, et al.
Human Genetics|April 1, 1997
Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's karyotype: a FISH analysisM Guttenbach, H W Michelmann, B Hinney, et al.
Human Genetics|April 1, 1997
Beta-thalassemia and beta[A] globin gene haplotypes in Mexican mestizosA R Villalobos-Arámbula, R Bustos, M Casas-Castañeda, et al.
Human Genetics|April 1, 1997
Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutationG Stevens, M Ramsay, T Jenkins
Human Genetics|April 1, 1997
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophyI Naom, M D'Alessandro, C Sewry, et al.
Human Genetics|April 1, 1997
The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2N J Lench, R Macadam, A F Markham
Human Genetics|September 22, 1977
Unusually long survival in a case of full triploidy of maternal originJ P Fryns, A van de Kerckhove, P Goddeeris, et al.
Pageof 957

Showing results (871-880 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|October 1, 1995
Detection of a C-insertion polymorphism within the human tumor necrosis factor alpha (TNFA) geneB M Brinkman, E L Kaijzel, T W Huizinga, et al.
Human Genetics|October 1, 1995
An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndromeN G Pasteris, J L Gorski
Human Genetics|October 1, 1995
Dinucleotide repeat polymorphism at the D5S99 locus on chromosome 5q33-34I M Groenewald, L Warnich, A E Retief
Human Genetics|April 1, 1997
Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophyE Kondo-Iida, K Saito, H Tanaka, et al.
Human Genetics|April 1, 1997
Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's karyotype: a FISH analysisM Guttenbach, H W Michelmann, B Hinney, et al.
Human Genetics|April 1, 1997
Beta-thalassemia and beta[A] globin gene haplotypes in Mexican mestizosA R Villalobos-Arámbula, R Bustos, M Casas-Castañeda, et al.
Human Genetics|April 1, 1997
Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutationG Stevens, M Ramsay, T Jenkins
Human Genetics|April 1, 1997
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophyI Naom, M D'Alessandro, C Sewry, et al.
Human Genetics|April 1, 1997
The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2N J Lench, R Macadam, A F Markham
Human Genetics|September 22, 1977
Unusually long survival in a case of full triploidy of maternal originJ P Fryns, A van de Kerckhove, P Goddeeris, et al.
Pageof 957