H H Ropers - JoVE Visualize

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Annals of Human Genetics|May 1, 1987

Physical mapping of genes and sequences at the end of the human X chromosome short armC Mondello, H H Ropers, I W Craig, et al.

Cytometry|November 1, 1984

Preparative dual-beam sorting of the human Y chromosome and in situ hybridization of cloned DNA probesC Cremer, G Rappold, J W Gray, et al.

Human Mutation|January 1, 1997

The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutationY J de Kok, C W Cremers, H H Ropers, et al.

Genomics|February 1, 1991

Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locusH J Smeets, R Hermens, H G Brunner, et al.

Human Molecular Genetics|November 11, 1999

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genomeN Blagitko, U Schulz, A A Schinzel, et al.

Human Genetics|January 1, 1995

Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB)W Berger, G van Duijnhoven, A Pinckers, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 8, 2001

UniGene cDNA array-based monitoring of transcriptome changes during mouse placental developmentM Hemberger, J C Cross, H H Ropers, et al.

Genomics|October 1, 1994

Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B)N Makita, K Sloan-Brown, D O Weghuis, et al.

Nature Genetics|September 1, 1993

The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humansV M Kalscheuer, E C Mariman, M T Schepens, et al.

Human Genetics|January 1, 1985

X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosomeU Friedrich, M Warburg, P Wieacker, et al.

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Showing results (41-50 of 204) with videos related to

Sort By:

Pageof 21

Annals of Human Genetics|May 1, 1987

Physical mapping of genes and sequences at the end of the human X chromosome short armC Mondello, H H Ropers, I W Craig, et al.

Cytometry|November 1, 1984

Preparative dual-beam sorting of the human Y chromosome and in situ hybridization of cloned DNA probesC Cremer, G Rappold, J W Gray, et al.

Human Mutation|January 1, 1997

The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutationY J de Kok, C W Cremers, H H Ropers, et al.

Genomics|February 1, 1991

Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locusH J Smeets, R Hermens, H G Brunner, et al.

Human Molecular Genetics|November 11, 1999

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genomeN Blagitko, U Schulz, A A Schinzel, et al.

Human Genetics|January 1, 1995

Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB)W Berger, G van Duijnhoven, A Pinckers, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 8, 2001

UniGene cDNA array-based monitoring of transcriptome changes during mouse placental developmentM Hemberger, J C Cross, H H Ropers, et al.

Genomics|October 1, 1994

Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B)N Makita, K Sloan-Brown, D O Weghuis, et al.

Nature Genetics|September 1, 1993

The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humansV M Kalscheuer, E C Mariman, M T Schepens, et al.

Human Genetics|January 1, 1985

X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosomeU Friedrich, M Warburg, P Wieacker, et al.

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