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Human genetics

Showing results (851-860 of 9,569) with videos related to

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Human Genetics|January 1, 1997
The T705I mutation of the low density lipoprotein receptor gene (FH Paris-9) does not cause familial hypercholesterolemiaP Lombardi, E J Sijbrands, S Kamerling, et al.
Human Genetics|January 1, 1997
Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contigA Jonasdottir, H Eiberg, B Kjer, et al.
Human Genetics|February 1, 1997
Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPPM Yamamoto, T Yasuda, K Hayasaka, et al.
Human Genetics|February 1, 1997
Two partial deletion mutations involving the same Alu sequence within intron 8 of the LDL receptor gene in Korean patients with familial hypercholesterolemiaJ J Chae, Y B Park, S H Kim, et al.
Human Genetics|February 1, 1997
Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteriaN E Beck, I P Tomlinson, T Homfray, et al.
Human Genetics|February 1, 1997
A high-frequency polymorphism of NADH-cytochrome b5 reductase in African-AmericansM M Jenkins, J T Prchal
Human Genetics|February 1, 1997
Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 regionA Toutain, N Ronce, B Dessay, et al.
Human Genetics|March 1, 1997
Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombinationJ Zucman-Rossi, M A Batzer, M Stoneking, et al.
Human Genetics|March 1, 1997
Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR)H H Lee, J G Chang, S P Lin, et al.
Human Genetics|March 1, 1997
Genomic organization and chromosomal localization of the human casein gene familyY Fujiwara, M Miwa, M Nogami, et al.
Pageof 957

Showing results (851-860 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|January 1, 1997
The T705I mutation of the low density lipoprotein receptor gene (FH Paris-9) does not cause familial hypercholesterolemiaP Lombardi, E J Sijbrands, S Kamerling, et al.
Human Genetics|January 1, 1997
Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contigA Jonasdottir, H Eiberg, B Kjer, et al.
Human Genetics|February 1, 1997
Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPPM Yamamoto, T Yasuda, K Hayasaka, et al.
Human Genetics|February 1, 1997
Two partial deletion mutations involving the same Alu sequence within intron 8 of the LDL receptor gene in Korean patients with familial hypercholesterolemiaJ J Chae, Y B Park, S H Kim, et al.
Human Genetics|February 1, 1997
Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteriaN E Beck, I P Tomlinson, T Homfray, et al.
Human Genetics|February 1, 1997
A high-frequency polymorphism of NADH-cytochrome b5 reductase in African-AmericansM M Jenkins, J T Prchal
Human Genetics|February 1, 1997
Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 regionA Toutain, N Ronce, B Dessay, et al.
Human Genetics|March 1, 1997
Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombinationJ Zucman-Rossi, M A Batzer, M Stoneking, et al.
Human Genetics|March 1, 1997
Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR)H H Lee, J G Chang, S P Lin, et al.
Human Genetics|March 1, 1997
Genomic organization and chromosomal localization of the human casein gene familyY Fujiwara, M Miwa, M Nogami, et al.
Pageof 957