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N C Nevin

Showing results (121-130 of 223) with videos related to

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American Journal of Medical Genetics|November 1, 1982
Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndromeN C Nevin, P S Thomas, J Calvert, et al.
Journal of Mental Deficiency Research|June 1, 1974
The Hallermann-Streiff syndromeN C Nevin, B G Scally, P Thomas, et al.
Journal of Medical Genetics|January 1, 1995
Detection of maternal cell contamination in amniotic fluid cell cultures using fluorescent labelled microsatellitesG W Smith, C A Graham, J Nevin, et al.
Proceedings of the Royal Society of Medicine|February 1, 1976
Effect of variation in alpha-1-antritrypsin phenotype upon incidence of respiratory illness in an unselected working populationR B Cole, N C Nevin, B L Bradley, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
A supernumerary chromosome 20, identified by FISH, in a male with azoospermia-cause or coincidence?S E McNerlan, Patrick J Morrison, N McClure, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The STR system in the human phenylalanine hydroxylase gene: true fragment length obtained with fluorescent labelled PCR primersJ Zschocke, C A Graham, J J McKnight, et al.
American Journal of Human Genetics|December 1, 1995
Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approachJ Zschocke, C A Graham, D J Carson, et al.
Human Genetics|August 1, 1997
Phenylketonuria and the peoples of Northern IrelandJ Zschocke, J P Mallory, H G Eiken, et al.
Genomics|April 1, 1992
Identification of a frameshift mutation (557 del T) in exon 4 of the CFTR geneC A Graham, P K Goon, A J Hill, et al.
American Journal of Medical Genetics|November 1, 1992
Cardiovascular abnormalities in the oculo-auriculo-vertebral spectrum (Goldenhar syndrome)P J Morrison, H C Mulholland, B G Craig, et al.
Pageof 23

Showing results (121-130 of 223) with videos related to

Sort By:
Pageof 23
American Journal of Medical Genetics|November 1, 1982
Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndromeN C Nevin, P S Thomas, J Calvert, et al.
Journal of Mental Deficiency Research|June 1, 1974
The Hallermann-Streiff syndromeN C Nevin, B G Scally, P Thomas, et al.
Journal of Medical Genetics|January 1, 1995
Detection of maternal cell contamination in amniotic fluid cell cultures using fluorescent labelled microsatellitesG W Smith, C A Graham, J Nevin, et al.
Proceedings of the Royal Society of Medicine|February 1, 1976
Effect of variation in alpha-1-antritrypsin phenotype upon incidence of respiratory illness in an unselected working populationR B Cole, N C Nevin, B L Bradley, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
A supernumerary chromosome 20, identified by FISH, in a male with azoospermia-cause or coincidence?S E McNerlan, Patrick J Morrison, N McClure, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The STR system in the human phenylalanine hydroxylase gene: true fragment length obtained with fluorescent labelled PCR primersJ Zschocke, C A Graham, J J McKnight, et al.
American Journal of Human Genetics|December 1, 1995
Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approachJ Zschocke, C A Graham, D J Carson, et al.
Human Genetics|August 1, 1997
Phenylketonuria and the peoples of Northern IrelandJ Zschocke, J P Mallory, H G Eiken, et al.
Genomics|April 1, 1992
Identification of a frameshift mutation (557 del T) in exon 4 of the CFTR geneC A Graham, P K Goon, A J Hill, et al.
American Journal of Medical Genetics|November 1, 1992
Cardiovascular abnormalities in the oculo-auriculo-vertebral spectrum (Goldenhar syndrome)P J Morrison, H C Mulholland, B G Craig, et al.
Pageof 23