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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 hyperphenylalaninaemia
J 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 tissues
L Stefani, J Galt, A Palmer, et al.
International Journal of Paediatric Dentistry
|
April 20, 2001
The KBG syndrome, characteristic dental findings: a case report
P A Dowling, P Fleming, R J Gorlin, et al.
The British Journal of Surgery
|
August 1, 1995
Hereditary breast cancer and linkage analysis to BRCA1
A 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 PKD1
G 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 Ireland
G 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 study
T R Tubman, M D Shields, B G Craig, et al.
Clinical Dysmorphology
|
April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiae
M Baraitser, F Stewart, R M Winter, et al.
The Ulster Medical Journal
|
November 1, 1996
Hereditary breast cancer in Northern Ireland
A 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 fibrosis
S A McMillan, A J Hill, C A Graham, et al.
Page
of 23
Search research articles
Search
Showing results (161-170 of 223) with videos related to
Sort By:
Page
of 23
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemia
J 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 tissues
L Stefani, J Galt, A Palmer, et al.
International Journal of Paediatric Dentistry
|
April 20, 2001
The KBG syndrome, characteristic dental findings: a case report
P A Dowling, P Fleming, R J Gorlin, et al.
The British Journal of Surgery
|
August 1, 1995
Hereditary breast cancer and linkage analysis to BRCA1
A 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 PKD1
G 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 Ireland
G 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 study
T R Tubman, M D Shields, B G Craig, et al.
Clinical Dysmorphology
|
April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiae
M Baraitser, F Stewart, R M Winter, et al.
The Ulster Medical Journal
|
November 1, 1996
Hereditary breast cancer in Northern Ireland
A 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 fibrosis
S A McMillan, A J Hill, C A Graham, et al.
Page
of 23