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Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
Medical problems in children with Down syndrome in the Erzurum area of Turkey
A Karaman
Genetic Counseling (Geneva, Switzerland)
|
February 7, 2012
Klippel-Feil syndrome and Dandy-Walker malformation
A Karaman, H Kahveci
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Unusual acrofacial dysostosis with severe limb defects: a new syndrome
A Karaman, H Kahveci
Genetic Counseling (Geneva, Switzerland)
|
October 23, 2010
A male newborn infant with fatco syndrome (fibular aplasia, tibial campomelia and oligodactyly): a case report
A Karaman, H Kahveci
The Journal of Emergency Medicine
|
May 25, 1999
Headache: cortical vein thrombosis and response to anticoagulation
J P Minadeo, B A Karaman
Genetic Counseling (Geneva, Switzerland)
|
June 6, 2015
Concomitant omphalocele, anencephaly and arthrogryposis associated with trisomy 18
A Karaman, H Aydin, K Göksu
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
A boy with Weyers-like ulnar ray/oligodactyly reduction limb defects and split hand malformation: case report
T Tos, A Karaman, D Gül
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 11, 2004
Parry-Romberg syndrome: a possible association with borreliosis
M T Sahin, S Bariş, A Karaman
International Journal of Dermatology
|
April 12, 2000
Lipoid proteinosis
K E Bozdağ, Y Gül, A Karaman
Folia Morphologica
|
January 4, 2018
The relationship between frontal sinus morphology and skeletal maturation
S K Buyuk, H Simsek, A Karaman
Page
of 6
Search research articles
Search
Showing results (1-10 of 58) with videos related to
Sort By:
Page
of 6
Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
Medical problems in children with Down syndrome in the Erzurum area of Turkey
A Karaman
Genetic Counseling (Geneva, Switzerland)
|
February 7, 2012
Klippel-Feil syndrome and Dandy-Walker malformation
A Karaman, H Kahveci
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
Unusual acrofacial dysostosis with severe limb defects: a new syndrome
A Karaman, H Kahveci
Genetic Counseling (Geneva, Switzerland)
|
October 23, 2010
A male newborn infant with fatco syndrome (fibular aplasia, tibial campomelia and oligodactyly): a case report
A Karaman, H Kahveci
The Journal of Emergency Medicine
|
May 25, 1999
Headache: cortical vein thrombosis and response to anticoagulation
J P Minadeo, B A Karaman
Genetic Counseling (Geneva, Switzerland)
|
June 6, 2015
Concomitant omphalocele, anencephaly and arthrogryposis associated with trisomy 18
A Karaman, H Aydin, K Göksu
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2011
A boy with Weyers-like ulnar ray/oligodactyly reduction limb defects and split hand malformation: case report
T Tos, A Karaman, D Gül
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 11, 2004
Parry-Romberg syndrome: a possible association with borreliosis
M T Sahin, S Bariş, A Karaman
International Journal of Dermatology
|
April 12, 2000
Lipoid proteinosis
K E Bozdağ, Y Gül, A Karaman
Folia Morphologica
|
January 4, 2018
The relationship between frontal sinus morphology and skeletal maturation
S K Buyuk, H Simsek, A Karaman
Page
of 6