Annals of human genetics - JoVE Visualize

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Annals of Human Genetics|May 1, 1986

Surnames in Sardinia. III. The spatial distribution of surnames for testing neutrality of genesG Zei, A Piazza, A Moroni, et al.

Annals of Human Genetics|October 1, 1986

EM investigations of surface spread synaptonemal complexes in a human male carrier of a pericentric inversion inv(13)(p12q14): the role of heterosynapsis for spermatocyte survivalN Saadallah, M Hultén

Annals of Human Genetics|October 1, 1986

Dermatoglyphic findings in fragile X syndrome: a causal hypothesis points to X-Y interchangeD Z Loesch

Annals of Human Genetics|December 16, 2004

Susceptibility to basal cell carcinoma: associations with PTCH polymorphismsR C Strange, N El-Genidy, S Ramachandran, et al.

Annals of Human Genetics|December 16, 2004

Linkage disequilibrium and haplotype architecture for two ABC transporter genes (ABCC1 and ABCG2) in Chinese population: implications for pharmacogenomic association studiesH Wang, B Hao, K Zhou, et al.

Annals of Human Genetics|December 16, 2004

DNA sequence variation and haplotype structure of the ICAM1 and TNF genes in 12 ethnic groups of India reveal patterns of importance in designing association studiesS Sengupta, S Farheen, N Mukherjee, et al.

Annals of Human Genetics|December 16, 2004

A tale of aborigines, conquerors and slaves: Alu insertion polymorphisms and the peopling of Canary IslandsN Maca-Meyer, J Villar, L Pérez-Méndez, et al.

Annals of Human Genetics|December 16, 2004

Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locusE Giardina, F Capon, M C De Rosa, et al.

Annals of Human Genetics|June 8, 2004

Notes on the maximum likelihood estimation of haplotype frequenciesS Mano, N Yasuda, T Katoh, et al.

Annals of Human Genetics|June 8, 2004

Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy populationM Adriani, A Martinez-Mir, F Fusco, et al.

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Showing results (1821-1830 of 2,305) with videos related to

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Pageof 231

Annals of Human Genetics|May 1, 1986

Surnames in Sardinia. III. The spatial distribution of surnames for testing neutrality of genesG Zei, A Piazza, A Moroni, et al.

Annals of Human Genetics|October 1, 1986

EM investigations of surface spread synaptonemal complexes in a human male carrier of a pericentric inversion inv(13)(p12q14): the role of heterosynapsis for spermatocyte survivalN Saadallah, M Hultén

Annals of Human Genetics|October 1, 1986

Dermatoglyphic findings in fragile X syndrome: a causal hypothesis points to X-Y interchangeD Z Loesch

Annals of Human Genetics|December 16, 2004

Susceptibility to basal cell carcinoma: associations with PTCH polymorphismsR C Strange, N El-Genidy, S Ramachandran, et al.

Annals of Human Genetics|December 16, 2004

Linkage disequilibrium and haplotype architecture for two ABC transporter genes (ABCC1 and ABCG2) in Chinese population: implications for pharmacogenomic association studiesH Wang, B Hao, K Zhou, et al.

Annals of Human Genetics|December 16, 2004

DNA sequence variation and haplotype structure of the ICAM1 and TNF genes in 12 ethnic groups of India reveal patterns of importance in designing association studiesS Sengupta, S Farheen, N Mukherjee, et al.

Annals of Human Genetics|December 16, 2004

A tale of aborigines, conquerors and slaves: Alu insertion polymorphisms and the peopling of Canary IslandsN Maca-Meyer, J Villar, L Pérez-Méndez, et al.

Annals of Human Genetics|December 16, 2004

Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locusE Giardina, F Capon, M C De Rosa, et al.

Annals of Human Genetics|June 8, 2004

Notes on the maximum likelihood estimation of haplotype frequenciesS Mano, N Yasuda, T Katoh, et al.

Annals of Human Genetics|June 8, 2004

Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy populationM Adriani, A Martinez-Mir, F Fusco, et al.

Pageof 231