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Human genetics

Showing results (801-810 of 9,569) with videos related to

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Human Genetics|January 11, 2003
Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytesFranck Pellestor, Brigitte Andréo, Françoise Arnal, et al.
Human Genetics|January 11, 2003
Maternal serum cell-free fetal DNA levels are increased in cases of trisomy 13 but not trisomy 18Tuangsit Wataganara, Erik S LeShane, Antonio Farina, et al.
Human Genetics|February 8, 2003
Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneityD U Braig, A A Schäffer, E Glocker, et al.
Human Genetics|February 8, 2003
Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)Jian Wang, Robert A Hegele
Human Genetics|April 15, 1976
Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13: report of three casesA Schinzel, K Hayashi, W Schmid
Human Genetics|April 15, 1976
Short arm deletion of an X chromosome, 46,XXp-P Kaiser, B Zabel, S Hansen, et al.
Human Genetics|March 11, 2003
The Finnish Disease Heritage III: the individual diseasesReijo Norio
Human Genetics|November 19, 2002
A novel approach for identifying candidate imprinted genes through sequence analysis of imprinted and control genesXiayi Ke, N Simon Thomas, David O Robinson, et al.
Human Genetics|July 24, 2002
Centromeric association of chromosome 16- and 18-derived microchromosomesUte Felbor, Désirée Rutschow, Thomas Haaf, et al.
Human Genetics|July 24, 2002
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafnessXiao Mei Ouyang, Xia Juan Xia, Elisabeth Verpy, et al.
Pageof 957

Showing results (801-810 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|January 11, 2003
Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytesFranck Pellestor, Brigitte Andréo, Françoise Arnal, et al.
Human Genetics|January 11, 2003
Maternal serum cell-free fetal DNA levels are increased in cases of trisomy 13 but not trisomy 18Tuangsit Wataganara, Erik S LeShane, Antonio Farina, et al.
Human Genetics|February 8, 2003
Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneityD U Braig, A A Schäffer, E Glocker, et al.
Human Genetics|February 8, 2003
Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)Jian Wang, Robert A Hegele
Human Genetics|April 15, 1976
Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13: report of three casesA Schinzel, K Hayashi, W Schmid
Human Genetics|April 15, 1976
Short arm deletion of an X chromosome, 46,XXp-P Kaiser, B Zabel, S Hansen, et al.
Human Genetics|March 11, 2003
The Finnish Disease Heritage III: the individual diseasesReijo Norio
Human Genetics|November 19, 2002
A novel approach for identifying candidate imprinted genes through sequence analysis of imprinted and control genesXiayi Ke, N Simon Thomas, David O Robinson, et al.
Human Genetics|July 24, 2002
Centromeric association of chromosome 16- and 18-derived microchromosomesUte Felbor, Désirée Rutschow, Thomas Haaf, et al.
Human Genetics|July 24, 2002
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafnessXiao Mei Ouyang, Xia Juan Xia, Elisabeth Verpy, et al.
Pageof 957