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Pediatric Dermatology
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February 24, 2001
Localized acquired hypertrichosis following cast application
A Kara, G Kanra, Y Alanay
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582)
R N Ergin, E Cigerciogullari, Y Alanay, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 11, 2008
Kabuki syndrome and trisomy 10p
G E Utine, Y Alanay, D Atkaş, et al.
Prenatal Diagnosis
|
July 3, 2007
Distal partial trisomy 1q: report of two cases and a review of the literature
G E Utine, D Aktas, Y Alanay, et al.
Lupus
|
February 9, 2016
Three cases of spondyloenchondrodysplasia (SPENCD) with systemic lupus erythematosus: a case series and review of the literature
Y Bilginer, A Düzova, R Topaloğlu, et al.
Molecular Syndromology
|
April 19, 2012
Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability
G E Utine, P Ö Kiper, Y Alanay, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 7, 2012
Opinions of Turkish physicians towards termination of pregnancy for fetal disorders
G E Utine, P O Kiper, B V Salanci, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2014
Parental factors in prenatal decision making and the impact of prenatal genetic counseling: a study on Turkish families
P O Simsek-Kiper, G E Utine, B Volkan-Salanci, et al.
Clinical Genetics
|
March 17, 2012
Clinical and molecular analysis of RASopathies in a group of Turkish patients
P Ö Şimşek-Kiper, Y Alanay, B Gülhan, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2013
Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome
G E Utine, B Akpınar, U Arslan, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Pediatric Dermatology
|
February 24, 2001
Localized acquired hypertrichosis following cast application
A Kara, G Kanra, Y Alanay
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582)
R N Ergin, E Cigerciogullari, Y Alanay, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 11, 2008
Kabuki syndrome and trisomy 10p
G E Utine, Y Alanay, D Atkaş, et al.
Prenatal Diagnosis
|
July 3, 2007
Distal partial trisomy 1q: report of two cases and a review of the literature
G E Utine, D Aktas, Y Alanay, et al.
Lupus
|
February 9, 2016
Three cases of spondyloenchondrodysplasia (SPENCD) with systemic lupus erythematosus: a case series and review of the literature
Y Bilginer, A Düzova, R Topaloğlu, et al.
Molecular Syndromology
|
April 19, 2012
Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability
G E Utine, P Ö Kiper, Y Alanay, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 7, 2012
Opinions of Turkish physicians towards termination of pregnancy for fetal disorders
G E Utine, P O Kiper, B V Salanci, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2014
Parental factors in prenatal decision making and the impact of prenatal genetic counseling: a study on Turkish families
P O Simsek-Kiper, G E Utine, B Volkan-Salanci, et al.
Clinical Genetics
|
March 17, 2012
Clinical and molecular analysis of RASopathies in a group of Turkish patients
P Ö Şimşek-Kiper, Y Alanay, B Gülhan, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2013
Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome
G E Utine, B Akpınar, U Arslan, et al.
Page
of 2