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N C Nevin

Showing results (181-190 of 223) with videos related to

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Occupational and Environmental Medicine|November 15, 2000
Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, IrelandG Dean, N C Nevin, M Mikkelsen, et al.
Health Technology Assessment (Winchester, England)|May 30, 2003
Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalitiesG M Grimshaw, A Szczepura, M Hultén, et al.
Prenatal Diagnosis|October 30, 1998
Laryngeal atresia or stenosis presenting as second-trimester fetal ascites--diagnosis and pathology in three independent casesP J Morrison, S Macphail, D Williams, et al.
Clinical Genetics|March 1, 1996
Wolcott-Rallison syndrome associated with congenital malformations and a mosaic deletion 15q 11-12F J Stewart, D J Carson, P S Thomas, et al.
Human Molecular Genetics|September 1, 1993
Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyriaD J Todd, A E Hughes, K T Ennis, et al.
Biochemical Society Transactions|April 1, 1990
Reduced secretion of specific proteins in dystrophic fibroblastsW H McLean, K Patel, A E Hughes, et al.
Human Mutation|January 1, 1996
Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomesD J Hughes, A J Hill, M Macek, et al.
The Quarterly Journal of Medicine|July 1, 1991
Gene probe analysis in an informative family with multiple endocrine neoplasia syndrome type 2A (MEN 2A). Improvement in carrier risk estimationP J Morrison, D R Hadden, A E Hughes, et al.
Thorax|April 1, 1976
Relation of alpha-1-antitrypsin phenotype to the performance of pulmonary function tests and to the prevalence of respiratory illness in a working populationR B Cole, N C Nevin, G Blundell, et al.
Pediatric Pathology|September 1, 1994
Congenital heart disease and urinary tract abnormalities in two siblings with DOOR syndromeC M Thornton, A C Magee, P S Thomas, et al.
Pageof 23

Showing results (181-190 of 223) with videos related to

Sort By:
Pageof 23
Occupational and Environmental Medicine|November 15, 2000
Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, IrelandG Dean, N C Nevin, M Mikkelsen, et al.
Health Technology Assessment (Winchester, England)|May 30, 2003
Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalitiesG M Grimshaw, A Szczepura, M Hultén, et al.
Prenatal Diagnosis|October 30, 1998
Laryngeal atresia or stenosis presenting as second-trimester fetal ascites--diagnosis and pathology in three independent casesP J Morrison, S Macphail, D Williams, et al.
Clinical Genetics|March 1, 1996
Wolcott-Rallison syndrome associated with congenital malformations and a mosaic deletion 15q 11-12F J Stewart, D J Carson, P S Thomas, et al.
Human Molecular Genetics|September 1, 1993
Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyriaD J Todd, A E Hughes, K T Ennis, et al.
Biochemical Society Transactions|April 1, 1990
Reduced secretion of specific proteins in dystrophic fibroblastsW H McLean, K Patel, A E Hughes, et al.
Human Mutation|January 1, 1996
Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomesD J Hughes, A J Hill, M Macek, et al.
The Quarterly Journal of Medicine|July 1, 1991
Gene probe analysis in an informative family with multiple endocrine neoplasia syndrome type 2A (MEN 2A). Improvement in carrier risk estimationP J Morrison, D R Hadden, A E Hughes, et al.
Thorax|April 1, 1976
Relation of alpha-1-antitrypsin phenotype to the performance of pulmonary function tests and to the prevalence of respiratory illness in a working populationR B Cole, N C Nevin, G Blundell, et al.
Pediatric Pathology|September 1, 1994
Congenital heart disease and urinary tract abnormalities in two siblings with DOOR syndromeC M Thornton, A C Magee, P S Thomas, et al.
Pageof 23