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B Say

Showing results (41-50 of 141) with videos related to

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The Turkish Journal of Pediatrics|January 1, 1974
Dermatoglyphic findings in familial coxa vara with dominant inheritanceM Atasu, K Tayşi, B Say
Clinical Genetics|January 1, 1974
Corneal opacity, microphthalmia, mental retardation, microcephaly and generalized muscular spasticity associated with hyperglycinemiaS Balci, B Say, T Firat
Acta Paediatrica Scandinavica|November 1, 1973
Letter: Multiple abnormalitiesS Yetkin, T Pirnar, B Say
Clinical Genetics|September 1, 1977
The Stickler syndrome (hereditary arthro-ophthalmopathy)B Say, J Berry, N Barber
Humangenetik|January 1, 1971
45,XO Turner's syndrome, Wilm's tumor and imprforate anusB Say, S Balci, E Tunçbilek
Human Heredity|January 1, 1974
Frequency of red cell adenosine deaminase and 6-phosphogluconate dehydrogenase in a sample of the Turkish populationC Altay, B Say, E Tuncbilek
Humangenetik|January 1, 1971
Laurence-Moon-Biedl syndrome in presumably identical twinsS Balci, B Say, R Erdal
Lancet (London, England)|October 14, 1972
Dermatoglyphics in trisomy 8E Tuncbilek, M Atasu, B Say
Lancet (London, England)|June 2, 1973
Hepatitis-associated antigen and Burkitt's lymphomaN Cevik, A Pirnar, B Say
Journal of Medical Genetics|January 1, 1996
Detection of a familial cryptic translocation by fluorescent in situ hybridisationD P Smith, M Floyd, B Say
Pageof 15

Showing results (41-50 of 141) with videos related to

Sort By:
Pageof 15
The Turkish Journal of Pediatrics|January 1, 1974
Dermatoglyphic findings in familial coxa vara with dominant inheritanceM Atasu, K Tayşi, B Say
Clinical Genetics|January 1, 1974
Corneal opacity, microphthalmia, mental retardation, microcephaly and generalized muscular spasticity associated with hyperglycinemiaS Balci, B Say, T Firat
Acta Paediatrica Scandinavica|November 1, 1973
Letter: Multiple abnormalitiesS Yetkin, T Pirnar, B Say
Clinical Genetics|September 1, 1977
The Stickler syndrome (hereditary arthro-ophthalmopathy)B Say, J Berry, N Barber
Humangenetik|January 1, 1971
45,XO Turner's syndrome, Wilm's tumor and imprforate anusB Say, S Balci, E Tunçbilek
Human Heredity|January 1, 1974
Frequency of red cell adenosine deaminase and 6-phosphogluconate dehydrogenase in a sample of the Turkish populationC Altay, B Say, E Tuncbilek
Humangenetik|January 1, 1971
Laurence-Moon-Biedl syndrome in presumably identical twinsS Balci, B Say, R Erdal
Lancet (London, England)|October 14, 1972
Dermatoglyphics in trisomy 8E Tuncbilek, M Atasu, B Say
Lancet (London, England)|June 2, 1973
Hepatitis-associated antigen and Burkitt's lymphomaN Cevik, A Pirnar, B Say
Journal of Medical Genetics|January 1, 1996
Detection of a familial cryptic translocation by fluorescent in situ hybridisationD P Smith, M Floyd, B Say
Pageof 15