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Journal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.Pediatric Hematology and Oncology|January 1, 1986
Short-time and low-dose intravenous acyclovir therapy in varicella zoster infections with malignant disease in children receiving combined chemotherapyF Sarialioğlu, M Buyukpamukcu, N Cevik, et al.American Journal of Medical Genetics|July 31, 1995
Partial trisomy 13q identified by sequential fluorescence in situ hybridizationV V Rao, N J Carpenter, M Gucsavas, et al.Annales De Genetique|January 1, 1996
Familial deletion of chromosome 18 (p11.2)G V Velagaleti, S Harris, N J Carpenter, et al.Acta Paediatrica Scandinavica|March 1, 1977
The radial dysplasia/imperforate anus/vertebral anomalies syndrome (the VATER association): Developmental aspects and eye findingsB Say, D Greenberg, R Harris, et al.Genetic Counseling (Geneva, Switzerland)|February 21, 2014
Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case reportB Say, N Guzoglu, N Uras, et al.The Journal of the Oklahoma State Medical Association|November 1, 1996
Charcot-Marie-Tooth disease type 1A: a family study with microsatellitesY Qu, N J Carpenter, L Whetsell, et al.Human Toxicology|March 1, 1987
Epidemiological aspects of childhood poisonings in Ankara: a 10-year surveyF Hincal, A A Hincal, Y Müftü, et al.Teratology|July 1, 1988
Split notochord syndrome with dorsal enteric fistula and sacral agenesisE L Kramer, G P Giacoia, B Say, et al.International Journal of Cardiology|May 4, 2001
The response of the myocardial metabolism to atrial pacing in patients with coronary slow flowB Yaymaci, S Dagdelen, N Bozbuga, et al.Pageof 7