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J Burn
T Strachan

Nature genetics

Showing results (1-10 of 14) with videos related to

Pageof 2
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Nature Genetics|September 1, 1995
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36S A Lynch, P M Bond, A J Copp, et al.
Nature Genetics|March 1, 1993
A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genomeS Collier, M Tassabehji, P Sinnott, et al.
Nature Genetics|June 1, 1997
A new dimension for the human genome project: towards comprehensive expression mapsT Strachan, M Abitbol, D Davidson, et al.
Nature Genetics|December 8, 1998
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesisA J Ross, V Ruiz-Perez, Y Wang, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.
Nature Genetics|December 1, 1995
Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor geneP J Biggs, R Wooster, D Ford, et al.
Nature Genetics|October 15, 1998
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouseD Morgan, L Turnpenny, J Goodship, et al.
Nature Genetics|November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3M Gebbia, G B Ferrero, G Pilia, et al.
Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Nature Genetics|September 1, 1995
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36S A Lynch, P M Bond, A J Copp, et al.
Nature Genetics|March 1, 1993
A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genomeS Collier, M Tassabehji, P Sinnott, et al.
Nature Genetics|June 1, 1997
A new dimension for the human genome project: towards comprehensive expression mapsT Strachan, M Abitbol, D Davidson, et al.
Nature Genetics|December 8, 1998
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesisA J Ross, V Ruiz-Perez, Y Wang, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.
Nature Genetics|December 1, 1995
Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor geneP J Biggs, R Wooster, D Ford, et al.
Nature Genetics|October 15, 1998
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouseD Morgan, L Turnpenny, J Goodship, et al.
Nature Genetics|November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3M Gebbia, G B Ferrero, G Pilia, et al.
Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
Pageof 2