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M L Budarf

Showing results (31-40 of 59) with videos related to

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American Journal of Human Genetics|July 25, 2000
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, E H Zackai, et al.
The Biochemical Journal|October 15, 1995
Structure of the human TIMP-3 gene and its cell cycle-regulated promoterM Wick, R Härönen, D Mumberg, et al.
Journal of Medical Genetics|October 1, 1993
Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defectsE Goldmuntz, D Driscoll, M L Budarf, et al.
Journal of Medical Genetics|October 1, 1993
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosisD A Driscoll, J Salvin, B Sellinger, et al.
The Journal of Biological Chemistry|September 6, 1996
Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndromeL B Ludlow, B P Schick, M L Budarf, et al.
Genomics|November 1, 1992
A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locusK A Frazer, M Boehnke, M L Budarf, et al.
DNA and Cell Biology|July 1, 1992
The human "peripheral-type" benzodiazepine receptor: regional mapping of the gene and characterization of the receptor expressed from cDNAY J Chang, R T McCabe, H Rennert, et al.
Genome Research|December 1, 1996
Long-range mapping and construction of a YAC contig within the cat eye syndrome critical regionH E McDermid, K E McTaggart, M A Riazi, et al.
Human Molecular Genetics|June 1, 1996
A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11W Gong, B S Emanuel, J Collins, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 2, 1999
Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human developmentT H Shaikh, S Gottlieb, B Sellinger, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|July 25, 2000
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, E H Zackai, et al.
The Biochemical Journal|October 15, 1995
Structure of the human TIMP-3 gene and its cell cycle-regulated promoterM Wick, R Härönen, D Mumberg, et al.
Journal of Medical Genetics|October 1, 1993
Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defectsE Goldmuntz, D Driscoll, M L Budarf, et al.
Journal of Medical Genetics|October 1, 1993
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosisD A Driscoll, J Salvin, B Sellinger, et al.
The Journal of Biological Chemistry|September 6, 1996
Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndromeL B Ludlow, B P Schick, M L Budarf, et al.
Genomics|November 1, 1992
A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locusK A Frazer, M Boehnke, M L Budarf, et al.
DNA and Cell Biology|July 1, 1992
The human "peripheral-type" benzodiazepine receptor: regional mapping of the gene and characterization of the receptor expressed from cDNAY J Chang, R T McCabe, H Rennert, et al.
Genome Research|December 1, 1996
Long-range mapping and construction of a YAC contig within the cat eye syndrome critical regionH E McDermid, K E McTaggart, M A Riazi, et al.
Human Molecular Genetics|June 1, 1996
A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11W Gong, B S Emanuel, J Collins, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 2, 1999
Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human developmentT H Shaikh, S Gottlieb, B Sellinger, et al.
Pageof 6