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Clinical Genetics
|
January 4, 2012
PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents
T Çelik, P O Simsek, T Sozen, 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.
Journal of Intellectual Disability Research : JIDR
|
February 19, 2019
An eight-case 1q21 region series: novel aberrations and clinical variability with new features
A C Ceylan, I Sahin, H B Erdem, 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.
Journal of Intellectual Disability Research : JIDR
|
March 19, 2021
Diagnostic yield of whole-exome sequencing in non-syndromic intellectual disability
E Z Taşkıran, B Karaosmanoğlu, C Koşukcu, 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.
Cytogenetic and Genome Research
|
September 29, 2007
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature
T Liehr, G E Utine, U Trautmann, et al.
Journal of Endocrinological Investigation
|
May 2, 2020
Genetic IGF1R defects: new cases expand the spectrum of clinical features
E N Gonc, Z A Ozon, S Oguz, et al.
Clinical Genetics
|
April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia
M Tekin, H Oztürkmen Akay, S Fitoz, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Clinical Genetics
|
January 4, 2012
PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents
T Çelik, P O Simsek, T Sozen, 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.
Journal of Intellectual Disability Research : JIDR
|
February 19, 2019
An eight-case 1q21 region series: novel aberrations and clinical variability with new features
A C Ceylan, I Sahin, H B Erdem, 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.
Journal of Intellectual Disability Research : JIDR
|
March 19, 2021
Diagnostic yield of whole-exome sequencing in non-syndromic intellectual disability
E Z Taşkıran, B Karaosmanoğlu, C Koşukcu, 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.
Cytogenetic and Genome Research
|
September 29, 2007
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature
T Liehr, G E Utine, U Trautmann, et al.
Journal of Endocrinological Investigation
|
May 2, 2020
Genetic IGF1R defects: new cases expand the spectrum of clinical features
E N Gonc, Z A Ozon, S Oguz, et al.
Clinical Genetics
|
April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia
M Tekin, H Oztürkmen Akay, S Fitoz, et al.
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of 2