Search research articles
Contact Us
Filters
Showing results (121-130 of 141) with videos related to
Page
of 15
Sort By:
American Journal of Medical Genetics
|
July 31, 1995
Partial trisomy 13q identified by sequential fluorescence in situ hybridization
V V Rao, N J Carpenter, M Gucsavas, et al.
Annales De Genetique
|
January 1, 1996
Familial deletion of chromosome 18 (p11.2)
G V Velagaleti, S Harris, N J Carpenter, et al.
Acta Paediatrica Scandinavica
|
March 1, 1977
The radial dysplasia/imperforate anus/vertebral anomalies syndrome (the VATER association): Developmental aspects and eye findings
B Say, D Greenberg, R Harris, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 21, 2014
Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report
B Say, N Guzoglu, N Uras, et al.
The Journal of the Oklahoma State Medical Association
|
November 1, 1996
Charcot-Marie-Tooth disease type 1A: a family study with microsatellites
Y Qu, N J Carpenter, L Whetsell, et al.
The Journal of Pediatrics
|
February 1, 1973
Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndrome
K Taysi, M Bobrow, S Balci, et al.
Human Heredity
|
January 1, 1973
Incidence of congenital malformations in a sample of the Turkish population
B Say, E Tunçbilek, S Balci, et al.
Teratology
|
July 1, 1988
Split notochord syndrome with dorsal enteric fistula and sacral agenesis
E L Kramer, G P Giacoia, B Say, et al.
International Journal of Cardiology
|
May 4, 2001
The response of the myocardial metabolism to atrial pacing in patients with coronary slow flow
B Yaymaci, S Dagdelen, N Bozbuga, et al.
The Turkish Journal of Pediatrics
|
July 1, 1973
Cervico-ocula-acusticus syndrome of Wildervanck. Case report
B Say, S Balci, R Israel, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 141) with videos related to
Sort By:
Page
of 15
American Journal of Medical Genetics
|
July 31, 1995
Partial trisomy 13q identified by sequential fluorescence in situ hybridization
V V Rao, N J Carpenter, M Gucsavas, et al.
Annales De Genetique
|
January 1, 1996
Familial deletion of chromosome 18 (p11.2)
G V Velagaleti, S Harris, N J Carpenter, et al.
Acta Paediatrica Scandinavica
|
March 1, 1977
The radial dysplasia/imperforate anus/vertebral anomalies syndrome (the VATER association): Developmental aspects and eye findings
B Say, D Greenberg, R Harris, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 21, 2014
Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report
B Say, N Guzoglu, N Uras, et al.
The Journal of the Oklahoma State Medical Association
|
November 1, 1996
Charcot-Marie-Tooth disease type 1A: a family study with microsatellites
Y Qu, N J Carpenter, L Whetsell, et al.
The Journal of Pediatrics
|
February 1, 1973
Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndrome
K Taysi, M Bobrow, S Balci, et al.
Human Heredity
|
January 1, 1973
Incidence of congenital malformations in a sample of the Turkish population
B Say, E Tunçbilek, S Balci, et al.
Teratology
|
July 1, 1988
Split notochord syndrome with dorsal enteric fistula and sacral agenesis
E L Kramer, G P Giacoia, B Say, et al.
International Journal of Cardiology
|
May 4, 2001
The response of the myocardial metabolism to atrial pacing in patients with coronary slow flow
B Yaymaci, S Dagdelen, N Bozbuga, et al.
The Turkish Journal of Pediatrics
|
July 1, 1973
Cervico-ocula-acusticus syndrome of Wildervanck. Case report
B Say, S Balci, R Israel, et al.
Page
of 15