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Human genetics

Showing results (991-1000 of 9,569) with videos related to

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Human Genetics|July 12, 1978
The occurrence of a ring 18, an accessory bisatellited fragment, and trisomy 21 within one sibshipE Grace, J Sills
Human Genetics|March 17, 2004
Parents of children with autosomal recessive diseases are not always carriers of the respective mutant allelesJoel Zlotogora
Human Genetics|March 27, 2004
Quasi-linkage: a confounding factor in linkage analysis of complex diseases?Sinthuja Sivagnanasundaram, Karl W Broman, Michelle Liu, et al.
Human Genetics|April 2, 2004
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicingJennifer Winter, Tanja Lehmann, Sybille Krauss, et al.
Human Genetics|March 5, 2004
A novel I247T missense mutation in the haptoglobin 2 beta-chain decreases the expression of the protein and is associated with ahaptoglobinemiaKwesi Teye, Isaac K E Quaye, Yoshiro Koda, et al.
Human Genetics|March 17, 1978
Kinetics of 21-trisomic lymphocytes. I. In vitro response of 21-trisomic lymphocytes to PHAA Serra, E Arpaia, R Bova
Human Genetics|January 30, 2004
Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndromeEiji Nakashima, Akihiko Mabuchi, Yoshio Makita, et al.
Human Genetics|December 1, 1992
On genetic components in autoimmunity: a critical review based on evolutionarily oriented rationalityJ T Epplen
Human Genetics|December 1, 1992
A familial mutation in the testis-determining gene SRY shared by both sexesR J Jäger, V R Harley, R A Pfeiffer, et al.
Human Genetics|December 1, 1992
Analysis of segregation and expression of an identified mutation at the neurofibromatosis type 1 locusM Stark, G Assum, D Kaufmann, et al.
Pageof 957

Showing results (991-1000 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|July 12, 1978
The occurrence of a ring 18, an accessory bisatellited fragment, and trisomy 21 within one sibshipE Grace, J Sills
Human Genetics|March 17, 2004
Parents of children with autosomal recessive diseases are not always carriers of the respective mutant allelesJoel Zlotogora
Human Genetics|March 27, 2004
Quasi-linkage: a confounding factor in linkage analysis of complex diseases?Sinthuja Sivagnanasundaram, Karl W Broman, Michelle Liu, et al.
Human Genetics|April 2, 2004
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicingJennifer Winter, Tanja Lehmann, Sybille Krauss, et al.
Human Genetics|March 5, 2004
A novel I247T missense mutation in the haptoglobin 2 beta-chain decreases the expression of the protein and is associated with ahaptoglobinemiaKwesi Teye, Isaac K E Quaye, Yoshiro Koda, et al.
Human Genetics|March 17, 1978
Kinetics of 21-trisomic lymphocytes. I. In vitro response of 21-trisomic lymphocytes to PHAA Serra, E Arpaia, R Bova
Human Genetics|January 30, 2004
Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndromeEiji Nakashima, Akihiko Mabuchi, Yoshio Makita, et al.
Human Genetics|December 1, 1992
On genetic components in autoimmunity: a critical review based on evolutionarily oriented rationalityJ T Epplen
Human Genetics|December 1, 1992
A familial mutation in the testis-determining gene SRY shared by both sexesR J Jäger, V R Harley, R A Pfeiffer, et al.
Human Genetics|December 1, 1992
Analysis of segregation and expression of an identified mutation at the neurofibromatosis type 1 locusM Stark, G Assum, D Kaufmann, et al.
Pageof 957