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Showing results (161-170 of 223) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemiaJ Zschocke, C A Graham, F J Stewart, et al.
Nucleic Acids Research|April 11, 1988
Expression of chromosome 21 specific sequences in normal and Down's syndrome tissuesL Stefani, J Galt, A Palmer, et al.
International Journal of Paediatric Dentistry|April 20, 2001
The KBG syndrome, characteristic dental findings: a case reportP A Dowling, P Fleming, R J Gorlin, et al.
The British Journal of Surgery|August 1, 1995
Hereditary breast cancer and linkage analysis to BRCA1A G McKinley, S E Russell, R A Spence, et al.
Journal of the American Society of Nephrology : JASN|October 1, 1994
Linkage disequilibrium between the CA microsatellite D16S283 and PKD1G D Wright, A E Hughes, K A Larkin, et al.
The Quarterly Journal of Medicine|July 1, 1993
Genetic linkage analysis, clinical features and prognosis of autosomal dominant polycystic kidney disease in Northern IrelandG D Wright, A E Hughes, K A Larkin, et al.
BMJ (Clinical Research Ed.)|June 15, 1991
Congenital heart disease in Down's syndrome: two year prospective early screening studyT R Tubman, M D Shields, B G Craig, et al.
Clinical Dysmorphology|April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiaeM Baraitser, F Stewart, R M Winter, et al.
The Ulster Medical Journal|November 1, 1996
Hereditary breast cancer in Northern IrelandA G McKinley, S E Russell, R A Spence, et al.
Journal of Medical Genetics|July 1, 1989
T cell receptor beta chain polymorphisms are associated with cystic fibrosisS A McMillan, A J Hill, C A Graham, et al.
Pageof 23

Showing results (161-170 of 223) with videos related to

Sort By:
Pageof 23
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemiaJ Zschocke, C A Graham, F J Stewart, et al.
Nucleic Acids Research|April 11, 1988
Expression of chromosome 21 specific sequences in normal and Down's syndrome tissuesL Stefani, J Galt, A Palmer, et al.
International Journal of Paediatric Dentistry|April 20, 2001
The KBG syndrome, characteristic dental findings: a case reportP A Dowling, P Fleming, R J Gorlin, et al.
The British Journal of Surgery|August 1, 1995
Hereditary breast cancer and linkage analysis to BRCA1A G McKinley, S E Russell, R A Spence, et al.
Journal of the American Society of Nephrology : JASN|October 1, 1994
Linkage disequilibrium between the CA microsatellite D16S283 and PKD1G D Wright, A E Hughes, K A Larkin, et al.
The Quarterly Journal of Medicine|July 1, 1993
Genetic linkage analysis, clinical features and prognosis of autosomal dominant polycystic kidney disease in Northern IrelandG D Wright, A E Hughes, K A Larkin, et al.
BMJ (Clinical Research Ed.)|June 15, 1991
Congenital heart disease in Down's syndrome: two year prospective early screening studyT R Tubman, M D Shields, B G Craig, et al.
Clinical Dysmorphology|April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiaeM Baraitser, F Stewart, R M Winter, et al.
The Ulster Medical Journal|November 1, 1996
Hereditary breast cancer in Northern IrelandA G McKinley, S E Russell, R A Spence, et al.
Journal of Medical Genetics|July 1, 1989
T cell receptor beta chain polymorphisms are associated with cystic fibrosisS A McMillan, A J Hill, C A Graham, et al.
Pageof 23