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European Journal of Medical Genetics
|
January 28, 2024
A spectrum of TP63-related disorders with eight affected individuals in five unrelated families
Merve Soğukpınar, Gülen Eda Utine, Koray Boduroğlu, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritance
Pelin Özlem Şimşek Kiper, Gülen Eda Utine, Koray Boduroğlu, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Partial distal aphalangia, duplication of metatarsal IV, microcephaly and borderline intelligence: a third patient suggesting autosomal recessive inheritance
Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş, et al.
American Journal of Medical Genetics. Part A
|
May 3, 2014
Barraquer-Simons syndrome: a rare clinical entity
Pelin Ozlem Simsek-Kiper, Emir Roach, Gulen Eda Utine, et al.
Pediatric Radiology
|
May 23, 2006
Terminal phalangeal accessory ossification center of the thumb: an additional radiographic finding in Larsen syndrome
Yasemin Alanay, Gulen Eda Utine, Ralph S Lachman, et al.
Experimental Eye Research
|
February 18, 2024
Allele-specific antisense oligonucleotides for the treatment of BEST1-related dominantly inherited retinal diseases: An in vitro model
Beren Karaosmanoglu, Gozde Imren, Eda Utine, et al.
The Turkish Journal of Pediatrics
|
August 20, 2010
Cowden syndrome with bronchial asthma
Yasemin Ozsürekci, Süleyman Tolga Yavuz, Yasemin Alanay, et al.
The Turkish Journal of Pediatrics
|
August 14, 2018
Anauxetic dysplasia: A rare clinical entity
Özlem Akgün-Doğan, Pelin Özlem Şimsek-Kiper, Gülen Eda Utine, et al.
European Journal of Medical Genetics
|
April 28, 2021
Three new cases of Crisponi /cold induced sweating syndrome (CS/CISS1) in Turkish families
Abdulkerim Kolkiran, Gizem Ürel-Demir, Pelin Özlem Şimşek-Kiper, et al.
American Journal of Medical Genetics. Part A
|
May 10, 2022
Diagnostic distribution and postnatal evaluation of prenatally detected short femur: A single center experience
Ayca Burcu Kahraman, Pelin Ozlem Simsek-Kiper, Gulen Eda Utine, et al.
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of 16
Search research articles
Search
Showing results (11-20 of 155) with videos related to
Sort By:
Page
of 16
European Journal of Medical Genetics
|
January 28, 2024
A spectrum of TP63-related disorders with eight affected individuals in five unrelated families
Merve Soğukpınar, Gülen Eda Utine, Koray Boduroğlu, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritance
Pelin Özlem Şimşek Kiper, Gülen Eda Utine, Koray Boduroğlu, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Partial distal aphalangia, duplication of metatarsal IV, microcephaly and borderline intelligence: a third patient suggesting autosomal recessive inheritance
Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş, et al.
American Journal of Medical Genetics. Part A
|
May 3, 2014
Barraquer-Simons syndrome: a rare clinical entity
Pelin Ozlem Simsek-Kiper, Emir Roach, Gulen Eda Utine, et al.
Pediatric Radiology
|
May 23, 2006
Terminal phalangeal accessory ossification center of the thumb: an additional radiographic finding in Larsen syndrome
Yasemin Alanay, Gulen Eda Utine, Ralph S Lachman, et al.
Experimental Eye Research
|
February 18, 2024
Allele-specific antisense oligonucleotides for the treatment of BEST1-related dominantly inherited retinal diseases: An in vitro model
Beren Karaosmanoglu, Gozde Imren, Eda Utine, et al.
The Turkish Journal of Pediatrics
|
August 20, 2010
Cowden syndrome with bronchial asthma
Yasemin Ozsürekci, Süleyman Tolga Yavuz, Yasemin Alanay, et al.
The Turkish Journal of Pediatrics
|
August 14, 2018
Anauxetic dysplasia: A rare clinical entity
Özlem Akgün-Doğan, Pelin Özlem Şimsek-Kiper, Gülen Eda Utine, et al.
European Journal of Medical Genetics
|
April 28, 2021
Three new cases of Crisponi /cold induced sweating syndrome (CS/CISS1) in Turkish families
Abdulkerim Kolkiran, Gizem Ürel-Demir, Pelin Özlem Şimşek-Kiper, et al.
American Journal of Medical Genetics. Part A
|
May 10, 2022
Diagnostic distribution and postnatal evaluation of prenatally detected short femur: A single center experience
Ayca Burcu Kahraman, Pelin Ozlem Simsek-Kiper, Gulen Eda Utine, et al.
Page
of 16