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Genetic Counseling (Geneva, Switzerland)
|
September 15, 2006
Mosaicism for terminal deletion of 4q
G E Utine, D Aktas
Genetic Counseling (Geneva, Switzerland)
|
January 31, 2006
Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1
G E Utine, C Melotte, J R Vermeesch, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 23, 2007
Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient
G E Utine, D Aktas, K Boduroğlu, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 2, 2005
Partial trisomy 11q syndrome (11q23.1-->11qter) due to de novo t (11q; 13q) detected by multicolor fluorescence in situ hybridisation
G E Utine, R Thoelen, H Peeters, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 11, 2008
Kabuki syndrome and trisomy 10p
G E Utine, Y Alanay, D Atkaş, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 25, 2013
Mucolipidosis type III in an adolescent presenting with atypical facial features and skeletal deformities
P O Simsek-Kiper, R Topaloglu, Y Sahin, 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.
Journal of Intellectual Disability Research : JIDR
|
October 18, 2021
Diagnostic yield of microarrays in individuals with non-syndromic developmental delay and intellectual disability
S Oğuz, U E Arslan, P Ö Ş Kiper, 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.
Page
of 2
Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Genetic Counseling (Geneva, Switzerland)
|
September 15, 2006
Mosaicism for terminal deletion of 4q
G E Utine, D Aktas
Genetic Counseling (Geneva, Switzerland)
|
January 31, 2006
Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1
G E Utine, C Melotte, J R Vermeesch, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 23, 2007
Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient
G E Utine, D Aktas, K Boduroğlu, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 2, 2005
Partial trisomy 11q syndrome (11q23.1-->11qter) due to de novo t (11q; 13q) detected by multicolor fluorescence in situ hybridisation
G E Utine, R Thoelen, H Peeters, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 11, 2008
Kabuki syndrome and trisomy 10p
G E Utine, Y Alanay, D Atkaş, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 25, 2013
Mucolipidosis type III in an adolescent presenting with atypical facial features and skeletal deformities
P O Simsek-Kiper, R Topaloglu, Y Sahin, 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.
Journal of Intellectual Disability Research : JIDR
|
October 18, 2021
Diagnostic yield of microarrays in individuals with non-syndromic developmental delay and intellectual disability
S Oğuz, U E Arslan, P Ö Ş Kiper, 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.
Page
of 2