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B Say

Showing results (71-80 of 141) with videos related to

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The Turkish Journal of Pediatrics|April 1, 1973
Dermatoglyphics in patients with a syndrome of brachydactyly, short stature and hypertensionK Taysi, M Atasu, B Say, et al.
American Journal of Medical Genetics|February 25, 1998
Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 caseF Schaefer, C Anderson, B Can, et al.
The Turkish Journal of Pediatrics|October 1, 1972
Giemsa banding patterns of 13/14, 21/21 translocations, Philadelphia chromosome and trisomy 18K Taysi, N Hatiboğlu, C Halicioglu, et al.
The Turkish Journal of Pediatrics|January 1, 1972
The heritability of liability to congenital dislocation of the hipM Atasu, U Akkoyunlu, N Tokgözoğlu, et al.
Birth Defects Original Article Series|January 1, 1979
Dwarfism associated with borderline intelligence, microcephaly, microphthalmia, and vertebral anomaliesN D Barber, B Say, J G Coldwell
Lancet (London, England)|November 10, 1973
Letter: Birth defects and oral contraceptivesS Balci, B Say, T Pirnar, et al.
JAMA|June 13, 1977
Anterior sacral meningoceleB Say, N J Carpenter, J G Coldwell
American Journal of Human Genetics|October 1, 1987
Prenatal studies in a family with transcobalamin II deficiencyJ S Mayes, B Say, D L Marcus
Acta Paediatrica Scandinavica|March 1, 1971
Oculodentodigital dysplasia syndromeK Taysi, B Say, T Firat, et al.
Lancet (London, England)|July 14, 1973
Dermatoglyphic findings in Laurence-Moon-Biedl syndromeM Atasu, S Balci, E Tuncbilek, et al.
Pageof 15

Showing results (71-80 of 141) with videos related to

Sort By:
Pageof 15
The Turkish Journal of Pediatrics|April 1, 1973
Dermatoglyphics in patients with a syndrome of brachydactyly, short stature and hypertensionK Taysi, M Atasu, B Say, et al.
American Journal of Medical Genetics|February 25, 1998
Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 caseF Schaefer, C Anderson, B Can, et al.
The Turkish Journal of Pediatrics|October 1, 1972
Giemsa banding patterns of 13/14, 21/21 translocations, Philadelphia chromosome and trisomy 18K Taysi, N Hatiboğlu, C Halicioglu, et al.
The Turkish Journal of Pediatrics|January 1, 1972
The heritability of liability to congenital dislocation of the hipM Atasu, U Akkoyunlu, N Tokgözoğlu, et al.
Birth Defects Original Article Series|January 1, 1979
Dwarfism associated with borderline intelligence, microcephaly, microphthalmia, and vertebral anomaliesN D Barber, B Say, J G Coldwell
Lancet (London, England)|November 10, 1973
Letter: Birth defects and oral contraceptivesS Balci, B Say, T Pirnar, et al.
JAMA|June 13, 1977
Anterior sacral meningoceleB Say, N J Carpenter, J G Coldwell
American Journal of Human Genetics|October 1, 1987
Prenatal studies in a family with transcobalamin II deficiencyJ S Mayes, B Say, D L Marcus
Acta Paediatrica Scandinavica|March 1, 1971
Oculodentodigital dysplasia syndromeK Taysi, B Say, T Firat, et al.
Lancet (London, England)|July 14, 1973
Dermatoglyphic findings in Laurence-Moon-Biedl syndromeM Atasu, S Balci, E Tuncbilek, et al.
Pageof 15