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Journal of Immunological Methods|September 9, 1996
A simplified, competitive RT-PCR method for measuring rat IFN-gamma mRNA expressionB Sun, J Wells, E Goldmuntz, et al.
Pediatric Cardiology|July 17, 2001
Patterns of right aortic arch and mirror-image branching of the brachiocephalic vessels without associated anomaliesD B McElhinney, A K Hoydu, J W Gaynor, et al.
Hepatology (Baltimore, Md.)|March 3, 1999
Features of Alagille syndrome in 92 patients: frequency and relation to prognosisK M Emerick, E B Rand, E Goldmuntz, et al.
Journal of Medical Genetics|October 1, 1993
Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defectsE Goldmuntz, D Driscoll, M L Budarf, et al.
American Journal of Medical Genetics|April 23, 1999
Jagged1 mutations in patients ascertained with isolated congenital heart defectsI D Krantz, R Smith, R P Colliton, et al.
Journal of the American College of Cardiology|June 23, 2001
Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branchingD B McElhinney, B J Clark, P M Weinberg, et al.
American Journal of Medical Genetics|November 15, 1993
DiGeorge anomaly with renal agenesis in infants of mothers with diabetesT A Wilson, S L Blethen, A Vallone, et al.
Pediatrics|May 11, 1997
Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetenceD M McDonald-McGinn, D A Driscoll, B S Emanuel, et al.
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