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A Child

Showing results (111-120 of 252) with videos related to

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American Journal of Medical Genetics|August 26, 1998
Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human developmentE S Park, E A Putnam, D Chitayat, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1994
Unrecognized dyslipoproteinemia in United Kingdom families recruited to a genetic register because of unexplained coronary heart diseaseA Staunton, D T Vallance, A Child, et al.
The British Journal of Ophthalmology|January 15, 2000
Visual loss after primary trabeculotomy with mitomycin C in Ehlers-Danlos syndromeM F Cordeiro, G T Plant, A Child, et al.
Histopathology|January 1, 1980
The histopathology of prolymphocytic leukaemia with particular reference to the spleen: a comparison with chronic lymphocytic leukaemiaI Lampert, D Catovsky, G W Marsh, et al.
Histopathology|September 1, 1985
Concurrent T-cell lymphocytic lymphoma and malignant histiocytosisC J O'Brien, J A Child, A Stark, et al.
Gastroenterology Research and Practice|August 29, 2018
Gastrointestinal Symptoms in Marfan Syndrome and Hypermobile Ehlers-Danlos SyndromeN Inayet, J O Hayat, A Kaul, et al.
Acta Haematologica|January 1, 1978
Evaluation of the usefulness of serum gamma-glutamyl transpeptidase levels in the management of haematological neoplasiaB E Roberts, J A Child, E H Cooper, et al.
The Biochemical Journal|September 15, 1994
Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndromeM Raghunath, C M Kielty, K Kainulainen, et al.
Circulation|November 24, 1999
Early and long-term results of a valve-sparing operation for Marfan syndromeE J Birks, C Webb, A Child, et al.
Ophthalmic Genetics|November 15, 1997
Identification of a new 'TIGR' mutation in a family with juvenile-onset primary open angle glaucomaD Stoilova, A Child, G Brice, et al.
Pageof 26

Showing results (111-120 of 252) with videos related to

Sort By:
Pageof 26
American Journal of Medical Genetics|August 26, 1998
Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human developmentE S Park, E A Putnam, D Chitayat, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1994
Unrecognized dyslipoproteinemia in United Kingdom families recruited to a genetic register because of unexplained coronary heart diseaseA Staunton, D T Vallance, A Child, et al.
The British Journal of Ophthalmology|January 15, 2000
Visual loss after primary trabeculotomy with mitomycin C in Ehlers-Danlos syndromeM F Cordeiro, G T Plant, A Child, et al.
Histopathology|January 1, 1980
The histopathology of prolymphocytic leukaemia with particular reference to the spleen: a comparison with chronic lymphocytic leukaemiaI Lampert, D Catovsky, G W Marsh, et al.
Histopathology|September 1, 1985
Concurrent T-cell lymphocytic lymphoma and malignant histiocytosisC J O'Brien, J A Child, A Stark, et al.
Gastroenterology Research and Practice|August 29, 2018
Gastrointestinal Symptoms in Marfan Syndrome and Hypermobile Ehlers-Danlos SyndromeN Inayet, J O Hayat, A Kaul, et al.
Acta Haematologica|January 1, 1978
Evaluation of the usefulness of serum gamma-glutamyl transpeptidase levels in the management of haematological neoplasiaB E Roberts, J A Child, E H Cooper, et al.
The Biochemical Journal|September 15, 1994
Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndromeM Raghunath, C M Kielty, K Kainulainen, et al.
Circulation|November 24, 1999
Early and long-term results of a valve-sparing operation for Marfan syndromeE J Birks, C Webb, A Child, et al.
Ophthalmic Genetics|November 15, 1997
Identification of a new 'TIGR' mutation in a family with juvenile-onset primary open angle glaucomaD Stoilova, A Child, G Brice, et al.
Pageof 26