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S Balci

Showing results (31-40 of 124) with videos related to

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Humangenetik|January 1, 1971
Laurence-Moon-Biedl syndrome in presumably identical twinsS Balci, B Say, R Erdal
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndromeO Kasaboğlu, C Tümer, S Balci
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Triphalangeal thumb in a case of VACTERL-hydrocephalus associationS Balci, M E Senocak, M Derbent
Clinical Genetics|December 8, 1998
Two brothers with hypospadias, hypertelorism, upper lid coloboma and mixed type hearing loss: a new syndromeS Balci, A Kayikcioglu, A S Dagli
Lancet (London, England)|July 14, 1973
Dermatoglyphic findings in Laurence-Moon-Biedl syndromeM Atasu, S Balci, E Tuncbilek, et al.
Clinical Genetics|June 1, 1997
A case of Carpenter syndrome diagnosed in a 20-week-old fetus with postmortem examinationS Balci, B Onol, M Eryilmaz, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 30, 1999
A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: coincidental finding or aetiological factor?V Baltaci, R Ors, M Kaya, et al.
American Journal of Medical Genetics|March 4, 2000
New syndrome?: Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cystsS Balci, S Bostanoğlu, G Altinok, et al.
The Turkish Journal of Pediatrics|July 1, 1980
Holt-Oram syndrome (analysis of six cases)E Tunçbilek, S Ozme, A Besim, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22)S Balci, O Engiz, Z Yilmaz, et al.
Pageof 13

Showing results (31-40 of 124) with videos related to

Sort By:
Pageof 13
Humangenetik|January 1, 1971
Laurence-Moon-Biedl syndrome in presumably identical twinsS Balci, B Say, R Erdal
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndromeO Kasaboğlu, C Tümer, S Balci
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Triphalangeal thumb in a case of VACTERL-hydrocephalus associationS Balci, M E Senocak, M Derbent
Clinical Genetics|December 8, 1998
Two brothers with hypospadias, hypertelorism, upper lid coloboma and mixed type hearing loss: a new syndromeS Balci, A Kayikcioglu, A S Dagli
Lancet (London, England)|July 14, 1973
Dermatoglyphic findings in Laurence-Moon-Biedl syndromeM Atasu, S Balci, E Tuncbilek, et al.
Clinical Genetics|June 1, 1997
A case of Carpenter syndrome diagnosed in a 20-week-old fetus with postmortem examinationS Balci, B Onol, M Eryilmaz, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 30, 1999
A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: coincidental finding or aetiological factor?V Baltaci, R Ors, M Kaya, et al.
American Journal of Medical Genetics|March 4, 2000
New syndrome?: Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cystsS Balci, S Bostanoğlu, G Altinok, et al.
The Turkish Journal of Pediatrics|July 1, 1980
Holt-Oram syndrome (analysis of six cases)E Tunçbilek, S Ozme, A Besim, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22)S Balci, O Engiz, Z Yilmaz, et al.
Pageof 13