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American Journal of Human Genetics|September 1, 1988
5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemiaG R Sutherland, E Baker, D F Callen, et al.Journal of the American College of Cardiology|December 1, 1990
Assessment of ventricular septal defect closure by intraoperative epicardial ultrasoundO Stümper, A G Fraser, N Elzenga, et al.Circulation|March 1, 1991
Safety of transesophageal echocardiography. A multicenter survey of 10,419 examinationsW G Daniel, R Erbel, W Kasper, et al.Biochimica Et Biophysica Acta|April 13, 2000
Y-receptor-like genes GPR72 and GPR73: molecular cloning, genomic organisation and assignment to human chromosome 11q21.1 and 2p14 and mouse chromosome 9 and 6R Parker, M Liu, H J Eyre, et al.American Journal of Human Genetics|January 1, 1990
Erythroid 5-aminolevulinate synthase is located on the X chromosomeT C Cox, M J Bawden, N G Abraham, et al.Nature|July 13, 1995
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2C Jones, L Penny, T Mattina, et al.British Heart Journal|October 1, 1992
Changes in left ventricular function and wall thickness in heart transplant recipients and their relation to acute rejection: an assessment by digitised M mode echocardiographyH F Mannaerts, A H Balk, M L Simoons, et al.Genes, Chromosomes & Cancer|February 1, 1994
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancerA M Cleton-Jansen, E W Moerland, N J Kuipers-Dijkshoorn, et al.Science (New York, N.Y.)|June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesisJ K Nancarrow, E Kremer, K Holman, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1991
An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15P J MacKinnon, B C Powell, G E Rogers, et al.Pageof 58