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A H Child

Showing results (1-10 of 45) with videos related to

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The Journal of Rheumatology|April 1, 1986
Joint hypermobility syndrome: inherited disorder of collagen synthesisA H Child
BMJ (Clinical Research Ed.)|January 11, 1992
Understanding Marfan's syndromeA H Child
British Medical Journal (Clinical Research Ed.)|June 11, 1988
Diagnosing Marfan's syndromeA H Child
Journal of Cardiac Surgery|March 1, 1997
Marfan syndrome--current medical and genetic knowledge: how to treat and whenA H Child
Birth Defects Original Article Series|January 1, 1977
The genetics of congenital heart diseaseA H Child, N R Dennis
Lancet (London, England)|February 9, 1980
Raised maternal serum alpha-fetoprotein, oligohydramnios, and the fetusM J Seller, A H Child
Angiology|May 4, 1999
Cause of primary congenital lymphedemaA H Child, J Beninson, M Sarfarazi
British Journal of Rheumatology|June 1, 1995
Assessment of bone mineral density in women with Marfan syndromeJ H Tobias, N Dalzell, A H Child
Human Mutation|April 17, 1999
The identification of five novel mutations in the lysosomal acid a-(1-4) glucosidase gene from patients with glycogen storage disease type II. Mutations in brief no. 134. OnlineC E Beesley, A H Child, M H Yacoub
Journal of the Royal Society of Medicine|August 1, 1988
Familial abdominal aortic aneurysmsT M Loosemore, A H Child, J A Dormandy
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
The Journal of Rheumatology|April 1, 1986
Joint hypermobility syndrome: inherited disorder of collagen synthesisA H Child
BMJ (Clinical Research Ed.)|January 11, 1992
Understanding Marfan's syndromeA H Child
British Medical Journal (Clinical Research Ed.)|June 11, 1988
Diagnosing Marfan's syndromeA H Child
Journal of Cardiac Surgery|March 1, 1997
Marfan syndrome--current medical and genetic knowledge: how to treat and whenA H Child
Birth Defects Original Article Series|January 1, 1977
The genetics of congenital heart diseaseA H Child, N R Dennis
Lancet (London, England)|February 9, 1980
Raised maternal serum alpha-fetoprotein, oligohydramnios, and the fetusM J Seller, A H Child
Angiology|May 4, 1999
Cause of primary congenital lymphedemaA H Child, J Beninson, M Sarfarazi
British Journal of Rheumatology|June 1, 1995
Assessment of bone mineral density in women with Marfan syndromeJ H Tobias, N Dalzell, A H Child
Human Mutation|April 17, 1999
The identification of five novel mutations in the lysosomal acid a-(1-4) glucosidase gene from patients with glycogen storage disease type II. Mutations in brief no. 134. OnlineC E Beesley, A H Child, M H Yacoub
Journal of the Royal Society of Medicine|August 1, 1988
Familial abdominal aortic aneurysmsT M Loosemore, A H Child, J A Dormandy
Pageof 5