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The Turkish Journal of Pediatrics
|
October 1, 1996
Tricho-rhino-phalangeal syndrome type I
Y Eroğlu, D Erçal
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 1, 1996
Sotos syndrome with septo-optic dysplasia
A Büyükgebiz, D Erçal, E Böber
Acta Paediatrica Japonica : Overseas Edition
|
October 1, 1995
Length polymorphism of heterochromatic segment of the Y chromosome in boys with acute leukemia
M D Erçal, K Bröndum-Nielsen
Clinical Dysmorphology
|
July 1, 1993
Robinow syndrome: with special emphasis on dermatoglyphics and hand malformations (split hand)
S Balci, M D Erçal, B Say, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 17, 2002
Amelogenesis imperfecta with growth hormone deficiency in a 12 year-old boy
B Dündar, D Erçal, E Böber, et al.
The Journal of Nihon University School of Dentistry
|
June 1, 1993
Neutrophil chemotaxis and periodontal status in Down's syndrome patients
E Yavuzyilmaz, F Ersoy, O Sanal, et al.
Clinical Dysmorphology
|
October 1, 1992
Three cases of oblique facial cleft: etiology, tomographic evaluation and reconstruction
E Mavili, G Gursu, M D Erçal, et al.
Clinical Genetics
|
April 1, 1991
Familial short rib syndrome, type Beemer, with pyloric stenosis and short intestine, one case diagnosed prenatally
S Balci, M D Erçal, B Onol, et al.
Clinical Dysmorphology
|
April 1, 1993
Autosomal recessive alobar holoprosencephaly with cyclops in three female sibs: prenatal ultrasonographic diagnosis at 18th week
S Balci, B Onol, M D Erçal, et al.
The Turkish Journal of Pediatrics
|
July 1, 1992
Meckel Gruber syndrome: a case diagnosed in utero
S Balci, B Onol, M D Erçal, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
The Turkish Journal of Pediatrics
|
October 1, 1996
Tricho-rhino-phalangeal syndrome type I
Y Eroğlu, D Erçal
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 1, 1996
Sotos syndrome with septo-optic dysplasia
A Büyükgebiz, D Erçal, E Böber
Acta Paediatrica Japonica : Overseas Edition
|
October 1, 1995
Length polymorphism of heterochromatic segment of the Y chromosome in boys with acute leukemia
M D Erçal, K Bröndum-Nielsen
Clinical Dysmorphology
|
July 1, 1993
Robinow syndrome: with special emphasis on dermatoglyphics and hand malformations (split hand)
S Balci, M D Erçal, B Say, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 17, 2002
Amelogenesis imperfecta with growth hormone deficiency in a 12 year-old boy
B Dündar, D Erçal, E Böber, et al.
The Journal of Nihon University School of Dentistry
|
June 1, 1993
Neutrophil chemotaxis and periodontal status in Down's syndrome patients
E Yavuzyilmaz, F Ersoy, O Sanal, et al.
Clinical Dysmorphology
|
October 1, 1992
Three cases of oblique facial cleft: etiology, tomographic evaluation and reconstruction
E Mavili, G Gursu, M D Erçal, et al.
Clinical Genetics
|
April 1, 1991
Familial short rib syndrome, type Beemer, with pyloric stenosis and short intestine, one case diagnosed prenatally
S Balci, M D Erçal, B Onol, et al.
Clinical Dysmorphology
|
April 1, 1993
Autosomal recessive alobar holoprosencephaly with cyclops in three female sibs: prenatal ultrasonographic diagnosis at 18th week
S Balci, B Onol, M D Erçal, et al.
The Turkish Journal of Pediatrics
|
July 1, 1992
Meckel Gruber syndrome: a case diagnosed in utero
S Balci, B Onol, M D Erçal, et al.
Page
of 2