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Human Heredity|January 1, 1980
Partial lipodystrophy and familial C3 deficiencyR H McLean, D HoefnagelJournal of Mental Deficiency Research|June 1, 1975
Banding identification of chromosomal abnormalities in four patients: ring (6), translocation (2q-;15q+), translocation (21q;21q) and deletion (22q-)D H Wurster-Hill, D HoefnagelClinical Pediatrics|March 1, 1983
Jejunal atresia associated with Cafergot ingestion during pregnancyJ M Graham, M Marin-Padilla, D HoefnagelAmerican Journal of Diseases of Children (1960)|August 1, 1979
Transient respiratory depression of the newborn. Its occurrence after succinylcholine administration to the motherD Hoefnagel, N A Harris, T H KimGenomics|November 1, 1989
A genetic linkage map of 32 loci on human chromosome 10D W Bowden, T C Gravius, P Green, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 1996
Acute myeloid leukemia-type chemotherapy for newly diagnosed patients without antecedent cytopenias having myelodysplastic syndrome as defined by French-American-British criteria: a Cancer and Leukemia Group B StudyS H Bernstein, V L Brunetto, F R Davey, et al.American Journal of Hematology|July 1, 1992
Morphologic characteristics of acute lymphoblastic leukemia (ALL) with abnormalities of chromosome 8, band q24F R Davey, D Lawrence, J MacCallum, et al.Acta Neurochirurgica|February 19, 2008
Risk factors for infections related to external ventricular drainageD Hoefnagel, R Dammers, M P Ter Laak-Poort, et al.American Journal of Medical Genetics|May 1, 1989
Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndromeU Tantravahi, R D Nicholls, H Stroh, et al.American Journal of Medical Genetics|May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndromeR D Nicholls, J H Knoll, K Glatt, et al.Pageof 2