Showing results (51-60 of 155) with videos related to
Sort By:
Pageof 16
Journal of Medical Genetics|June 1, 1981
An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?N J Carpenter, L G Leichtman, S Stamper, et al.Journal of Medical Genetics|August 1, 1986
Microcephaly, short stature, and developmental delay associated with a chemotactic defect and transient hypogammaglobulinaemia in two brothersB Say, N Barber, G C Miller, et al.American Journal of Medical Genetics|March 13, 1995
CD1+ cells in mothers of stillborn infants with neural tube defectsF N Seniz, E Müftüoğlu, M S Batun, et al.The Journal of the Oklahoma State Medical Association|March 21, 1998
Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosisB Can, F V Schaefer, S Malik, et al.Journal of Medical Genetics|November 1, 1987
Partial deletion 21: case report with biochemical studies and reviewN J Carpenter, J S Mayes, B Say, et al.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.British Journal of Haematology|November 1, 1992
Homozygosity for dominant form of hereditary spherocytosisF Duru, A Gürgey, G Oztürk, et al.Nucleic Acids Research|September 25, 1984
Two novel arrangements of the human fetal globin genes: G gamma-G gamma and A gamma-A gammaP A Powers, C Altay, T H Huisman, et al.The Turkish Journal of Pediatrics|January 1, 1990
Acute lymphoblastic leukemia in a child with hemoglobins S and Q-IranA Gürgey, S Ozsoylu, G Hiçsönmez, et al.Journal of Medicine|January 1, 1994
Chronic autoimmune hemolytic anemia in children: a report of four patientsF Duru, A Gürgey, M Cetin, et al.Pageof 16