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Human genetics

Showing results (841-850 of 9,569) with videos related to

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Human Genetics|August 1, 1993
Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1E C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.
Human Genetics|August 31, 1977
Chromosomes 1 in 14 ovarian cancers. Heterochromatin variants and structural changesN B Atkin, V J Pickthall
Human Genetics|August 31, 1977
Classification of qh regions in human chromosomes 1, 9, and 16 by C-bandingS R Patil, H A Lubs
Human Genetics|January 1, 1997
Refined molecular characterization of the breakpoints in small inv dup(15) chromosomesB Huang, J A Crolla, S L Christian, et al.
Human Genetics|January 1, 1997
Molecular evidence for human alpha 2-HS glycoprotein (AHSG) polymorphismM Osawa, K Umetsu, T Ohki, et al.
Human Genetics|January 1, 1997
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex familiesD F Wyszynski, N Maestri, I McIntosh, et al.
Human Genetics|January 1, 1997
Allelic variants of human calcitonin receptor in the Japanese populationM Nakamura, Z Q Zhang, L Shan, et al.
Human Genetics|January 1, 1997
Prevalence of delta F508 cystic fibrosis carriers in The Netherlands: logistic regression on sex, age, region of residence and number of offspringH G de Vries, J M Collée, H E de Walle, et al.
Human Genetics|January 1, 1997
X-linked adrenal hypoplasia in a large Greenlandic family. Detection of a missense mutation (N4401) in the DAX-1 gene; implication for genetic counselling and carrier diagnosisM Schwartz, S Blichfeldt, J Müller
Human Genetics|January 1, 1997
The high mobility group I-C gene (HMGI-C): polymorphism and genetic localizationC S Ishwad, M D Shriver, D M Lassige, et al.
Pageof 957

Showing results (841-850 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|August 1, 1993
Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1E C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.
Human Genetics|August 31, 1977
Chromosomes 1 in 14 ovarian cancers. Heterochromatin variants and structural changesN B Atkin, V J Pickthall
Human Genetics|August 31, 1977
Classification of qh regions in human chromosomes 1, 9, and 16 by C-bandingS R Patil, H A Lubs
Human Genetics|January 1, 1997
Refined molecular characterization of the breakpoints in small inv dup(15) chromosomesB Huang, J A Crolla, S L Christian, et al.
Human Genetics|January 1, 1997
Molecular evidence for human alpha 2-HS glycoprotein (AHSG) polymorphismM Osawa, K Umetsu, T Ohki, et al.
Human Genetics|January 1, 1997
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex familiesD F Wyszynski, N Maestri, I McIntosh, et al.
Human Genetics|January 1, 1997
Allelic variants of human calcitonin receptor in the Japanese populationM Nakamura, Z Q Zhang, L Shan, et al.
Human Genetics|January 1, 1997
Prevalence of delta F508 cystic fibrosis carriers in The Netherlands: logistic regression on sex, age, region of residence and number of offspringH G de Vries, J M Collée, H E de Walle, et al.
Human Genetics|January 1, 1997
X-linked adrenal hypoplasia in a large Greenlandic family. Detection of a missense mutation (N4401) in the DAX-1 gene; implication for genetic counselling and carrier diagnosisM Schwartz, S Blichfeldt, J Müller
Human Genetics|January 1, 1997
The high mobility group I-C gene (HMGI-C): polymorphism and genetic localizationC S Ishwad, M D Shriver, D M Lassige, et al.
Pageof 957