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The Turkish Journal of Pediatrics
|
January 1, 1983
Absence of a hand (acheiria) in a child whose father was treated with cyclophosphamide for Behçet's disease
S Balci, F Sarikayalar
The Turkish Journal of Pediatrics
|
October 1, 1971
Hallermann-Streiff syndrome. (Dyscephalia mandibulo-oculo-facialis)
S Balci, B Say
Genetic Counseling (Geneva, Switzerland)
|
August 23, 2007
Co-occurrence of familial Mediterranean fever (FMF) heterozygote mutation and nail-patella syndrome (NPS) in 3 members of a family with LMX1B mutation analysis
S Balci, O Engiz
Clinical Dysmorphology
|
October 23, 2001
Cri-du-chat syndrome associated with arachnoid cyst causing triventricular hydrocephalus
S Balci, K K Oguz
Clinical Genetics
|
April 1, 1993
Can cytomegalovirus cause brachydactyly? A case report and review of the literature
M Cinbis, M Topcu, S Balci
The Turkish Journal of Pediatrics
|
July 1, 1970
Werner's syndrome
S Balci, B Say, E Kinik
Progress in Clinical and Biological Research
|
January 1, 1982
A case of SC-phocomelia syndrome with nonrandom centromere separation
I Bökesoy, S Balci, S Bilgiç
The Turkish Journal of Pediatrics
|
July 1, 1982
Short-rib-polydactyly syndrome (Saldino-Noonan type)
T Pirnar, S Balci, M Cağlar
The Turkish Journal of Pediatrics
|
October 9, 1998
A case of a four-day-old male with Carpenter's syndrome with transposition of great arteries
S Balci, T Haytoğlu, S Ozer
The Turkish Journal of Pediatrics
|
January 5, 2002
Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly
S Balci, K Boduroğlu, S Kaya
Page
of 13
Search research articles
Search
Showing results (11-20 of 124) with videos related to
Sort By:
Page
of 13
The Turkish Journal of Pediatrics
|
January 1, 1983
Absence of a hand (acheiria) in a child whose father was treated with cyclophosphamide for Behçet's disease
S Balci, F Sarikayalar
The Turkish Journal of Pediatrics
|
October 1, 1971
Hallermann-Streiff syndrome. (Dyscephalia mandibulo-oculo-facialis)
S Balci, B Say
Genetic Counseling (Geneva, Switzerland)
|
August 23, 2007
Co-occurrence of familial Mediterranean fever (FMF) heterozygote mutation and nail-patella syndrome (NPS) in 3 members of a family with LMX1B mutation analysis
S Balci, O Engiz
Clinical Dysmorphology
|
October 23, 2001
Cri-du-chat syndrome associated with arachnoid cyst causing triventricular hydrocephalus
S Balci, K K Oguz
Clinical Genetics
|
April 1, 1993
Can cytomegalovirus cause brachydactyly? A case report and review of the literature
M Cinbis, M Topcu, S Balci
The Turkish Journal of Pediatrics
|
July 1, 1970
Werner's syndrome
S Balci, B Say, E Kinik
Progress in Clinical and Biological Research
|
January 1, 1982
A case of SC-phocomelia syndrome with nonrandom centromere separation
I Bökesoy, S Balci, S Bilgiç
The Turkish Journal of Pediatrics
|
July 1, 1982
Short-rib-polydactyly syndrome (Saldino-Noonan type)
T Pirnar, S Balci, M Cağlar
The Turkish Journal of Pediatrics
|
October 9, 1998
A case of a four-day-old male with Carpenter's syndrome with transposition of great arteries
S Balci, T Haytoğlu, S Ozer
The Turkish Journal of Pediatrics
|
January 5, 2002
Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly
S Balci, K Boduroğlu, S Kaya
Page
of 13