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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.
Clinical and Experimental Pharmacology & Physiology|October 9, 2002
Transforming growth factor-beta 1 does not relate to hypertension in pre-eclampsiaA Hennessy, S Orange, N Willis, et al.
Spine|July 1, 2014
Vertebral artery anomalies at the craniovertebral junction in the US populationCourtney M OʼDonnell, Zachary A Child, Quynh Nguyen, et al.
Archives of Biochemistry and Biophysics|March 2, 2024
Structural determination and characterisation of the CYP105Q4 cytochrome P450 enzyme from Mycobacterium marinumHebatalla Mohamed, Stella A Child, Daniel Z Doherty, et al.
Australian and New Zealand Journal of Medicine|April 1, 1989
Very high dose intravenous gammaglobulin in thrombocytopenia of pregnancyJ Gibson, P P Laird, D E Joshua, et al.
Royal Society Open Science|March 20, 2025
Developing the evidence-base to inform policy on inclusive research designStella A Child, Christina Mulligan, Ivan Pavlov, et al.
Gut|August 1, 1973
The diagnosis of iron deficiency in patients with Crohn's diseaseJ A Child, B Brozović, N H Dyer, et al.
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