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B Say

Showing results (101-110 of 141) with videos related to

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The Journal of Pediatrics|May 1, 1979
Association of birth defects and immunodeficiencyB Say, G C Miller, N Barber, et al.
The Turkish Journal of Pediatrics|July 1, 1971
13-15 (D1) trisomy syndrome. (With special emphasis on pathological findings)E Tun cbilek, S Balci, B Say, et al.
Acta Haematologica|January 1, 1973
Hereditary persistence of fetal hemoglobin and beta-thalassemia in a Turkish childB Yamak, S Ozsoylu, C Altay, et al.
Clinical Pediatrics|December 1, 1982
A condition resembling congenital hypoplastic anemia occurring in a mother and sonG McFarland, B Say, N J Carpenter, et al.
The Turkish Journal of Pediatrics|July 1, 1994
Aase-Smith syndrome: report of a new case with unusual featuresS Yetgin, S Balci, G Irken, et al.
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.
The Journal of Bone and Joint Surgery. British Volume|February 1, 1974
Dominant congenital coxa varaB Say, K Taysi, T Pirnar, et al.
Humangenetik|January 1, 1975
A new dominantly inherited syndrome of cleft palateB Say, D H Barber, J Hobbs, et al.
Clinical Pediatrics|April 1, 1976
Goodpasture's syndrome (pulmonary hemosiderosis with nephritis)S Ozsoylu, G Hicsonmez, I Berkel, 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.
Pageof 15

Showing results (101-110 of 141) with videos related to

Sort By:
Pageof 15
The Journal of Pediatrics|May 1, 1979
Association of birth defects and immunodeficiencyB Say, G C Miller, N Barber, et al.
The Turkish Journal of Pediatrics|July 1, 1971
13-15 (D1) trisomy syndrome. (With special emphasis on pathological findings)E Tun cbilek, S Balci, B Say, et al.
Acta Haematologica|January 1, 1973
Hereditary persistence of fetal hemoglobin and beta-thalassemia in a Turkish childB Yamak, S Ozsoylu, C Altay, et al.
Clinical Pediatrics|December 1, 1982
A condition resembling congenital hypoplastic anemia occurring in a mother and sonG McFarland, B Say, N J Carpenter, et al.
The Turkish Journal of Pediatrics|July 1, 1994
Aase-Smith syndrome: report of a new case with unusual featuresS Yetgin, S Balci, G Irken, et al.
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.
The Journal of Bone and Joint Surgery. British Volume|February 1, 1974
Dominant congenital coxa varaB Say, K Taysi, T Pirnar, et al.
Humangenetik|January 1, 1975
A new dominantly inherited syndrome of cleft palateB Say, D H Barber, J Hobbs, et al.
Clinical Pediatrics|April 1, 1976
Goodpasture's syndrome (pulmonary hemosiderosis with nephritis)S Ozsoylu, G Hicsonmez, I Berkel, 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.
Pageof 15