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American Journal of Medical Genetics|February 1, 1989
Syndrome of imperforate oropharynx with costovertebral and auricular anomaliesD B FlanneryActa Geneticae Medicae Et Gemellologiae|January 1, 1987
The possible role of homeotic genes in the causation of malformations in monozygotic twinsD B FlannerySouthern Medical Journal|October 1, 1985
Surgical aspects of limb deformity in hypophosphatemic ricketsW B Greene, S G KahlerThe Journal of Biological Chemistry|January 25, 1983
Intracellular glucose-6-phosphate dehydrogenase does not monomerize in human erythrocytesS G Kahler, H N KirkmanSouthern Medical Journal|October 1, 1985
Hypophosphatemic rickets: still misdiagnosed and inadequately treatedW B Greene, S G KahlerClinical Genetics|June 1, 1986
Craniofrontonasal dysplasia: clinical and genetic analysisC M Sax, D B FlanneryPrenatal Diagnosis|January 1, 1985
Tests appropriate for the prenatal diagnosis of ataxia telangiectasiaS Schwartz, D B Flannery, M M CohenAmerican Journal of Medical Genetics|February 1, 1984
A mild autosomal recessive form of osteopetrosisS G Kahler, J A Burns, A S AylsworthActa Paediatrica Scandinavica|November 1, 1991
Brain abscess in glycogen storage disease type IbH K Park, S G Kahler, Y T ChenPageof 7