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Pediatric Hematology and Oncology|September 1, 1994
Convulsion after blood transfusion in four beta-thalassemia intermedia patientsA Gürgey, O Kalayci, F Gümrük, 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.
British Journal of Haematology|February 23, 1999
Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous familyA Koc, J C Pronk, M Alikasifoglu, et al.
Pediatric Research|August 1, 1981
alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemiaC Altay, M E Gravely, B R Joseph, et al.
Thrombosis Research|March 15, 2001
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and KyrgyzstanG Balta, A Gurgey, D K Kudayarov, et al.
American Journal of Hematology|July 1, 1990
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genesC Oner, A Gurgey, C Altay, et al.
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