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A H Child

Showing results (11-20 of 45) with videos related to

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Birth Defects Original Article Series|January 1, 1974
Hypoplastic left heart. Evidence for possible autosomal recessive inheritance. CommentL B Holmes, V Rose, A H Child, et al.
Thorax|October 1, 1984
Pulmonary disease in patients with Marfan syndromeJ R Wood, D Bellamy, A H Child, et al.
Human Mutation|December 19, 2001
Erratum: Detection of six novel FBN1 mutations in British patients affected by Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.
Human Mutation|August 29, 2001
Detection of six novel FBN1 mutations in British patients affected by Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.
Eye (London, England)|October 7, 2006
The -174G/C interleukin-6 promoter polymorphism influences the development of macular oedema following uncomplicated phacoemulsification surgeryI Masood, A Negi, S A Vernon, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 geneN H Elçioglu, F Akalin, M Elçioglu, et al.
The Journal of Infectious Diseases|February 18, 1998
Limulus antilipopolysaccharide factor prevents mortality late in the course of endotoxemiaR I Roth, D Su, A H Child, et al.
The British Journal of Ophthalmology|November 26, 2002
Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitusP Comeglio, A L Evans, G Brice, et al.
Journal of Cell Science|March 1, 1995
Cysteine-to-arginine point mutation in a 'hybrid' eight-cysteine domain of FBN1: consequences for fibrillin aggregation and microfibril assemblyC M Kielty, T Rantamäki, A H Child, et al.
The Journal of Rheumatology|September 16, 2000
Fibromyalgia, hypermobility, and breast implantsS Lai, J A Goldman, A H Child, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Birth Defects Original Article Series|January 1, 1974
Hypoplastic left heart. Evidence for possible autosomal recessive inheritance. CommentL B Holmes, V Rose, A H Child, et al.
Thorax|October 1, 1984
Pulmonary disease in patients with Marfan syndromeJ R Wood, D Bellamy, A H Child, et al.
Human Mutation|December 19, 2001
Erratum: Detection of six novel FBN1 mutations in British patients affected by Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.
Human Mutation|August 29, 2001
Detection of six novel FBN1 mutations in British patients affected by Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.
Eye (London, England)|October 7, 2006
The -174G/C interleukin-6 promoter polymorphism influences the development of macular oedema following uncomplicated phacoemulsification surgeryI Masood, A Negi, S A Vernon, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 geneN H Elçioglu, F Akalin, M Elçioglu, et al.
The Journal of Infectious Diseases|February 18, 1998
Limulus antilipopolysaccharide factor prevents mortality late in the course of endotoxemiaR I Roth, D Su, A H Child, et al.
The British Journal of Ophthalmology|November 26, 2002
Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitusP Comeglio, A L Evans, G Brice, et al.
Journal of Cell Science|March 1, 1995
Cysteine-to-arginine point mutation in a 'hybrid' eight-cysteine domain of FBN1: consequences for fibrillin aggregation and microfibril assemblyC M Kielty, T Rantamäki, A H Child, et al.
The Journal of Rheumatology|September 16, 2000
Fibromyalgia, hypermobility, and breast implantsS Lai, J A Goldman, A H Child, et al.
Pageof 5