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B J Trask

Showing results (61-70 of 74) with videos related to

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Genomics|July 1, 1992
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17pV Guzzetta, B Franco, B J Trask, et al.
Nucleic Acids Research|May 11, 1992
Isolation and characterization of the cDNA encoding human DNA methyltransferaseR W Yen, P M Vertino, B D Nelkin, et al.
American Journal of Medical Genetics|September 11, 1995
Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridizationR C Juyal, F Greenberg, G A Mengden, et al.
Nature Genetics|May 1, 1992
Evolution of the mammalian G protein alpha subunit multigene familyT M Wilkie, D J Gilbert, A S Olsen, et al.
Nature Genetics|October 1, 1993
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, L Pentao, et al.
Nature Genetics|June 1, 1992
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1AP I Patel, B B Roa, A A Welcher, et al.
Cell|July 26, 1991
DNA duplication associated with Charcot-Marie-Tooth disease type 1AJ R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.
Human Molecular Genetics|March 21, 1998
Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancersT H Thai, F Du, J T Tsan, et al.
Human Genetics|December 1, 1996
Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patientsB J Trask, H Mefford, G van den Engh, et al.
Human Molecular Genetics|June 13, 1998
Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instabilityA R La Spada, K R Peterson, S A Meadows, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Genomics|July 1, 1992
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17pV Guzzetta, B Franco, B J Trask, et al.
Nucleic Acids Research|May 11, 1992
Isolation and characterization of the cDNA encoding human DNA methyltransferaseR W Yen, P M Vertino, B D Nelkin, et al.
American Journal of Medical Genetics|September 11, 1995
Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridizationR C Juyal, F Greenberg, G A Mengden, et al.
Nature Genetics|May 1, 1992
Evolution of the mammalian G protein alpha subunit multigene familyT M Wilkie, D J Gilbert, A S Olsen, et al.
Nature Genetics|October 1, 1993
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, L Pentao, et al.
Nature Genetics|June 1, 1992
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1AP I Patel, B B Roa, A A Welcher, et al.
Cell|July 26, 1991
DNA duplication associated with Charcot-Marie-Tooth disease type 1AJ R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.
Human Molecular Genetics|March 21, 1998
Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancersT H Thai, F Du, J T Tsan, et al.
Human Genetics|December 1, 1996
Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patientsB J Trask, H Mefford, G van den Engh, et al.
Human Molecular Genetics|June 13, 1998
Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instabilityA R La Spada, K R Peterson, S A Meadows, et al.
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