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G Eda Utine

Showing results (1-10 of 14) with videos related to

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European Journal of Medical Genetics|February 14, 2006
Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogueG Eda Utine, Ayfer Alikasifoglu, Mehmet Alikasifoglu, et al.
The Turkish Journal of Pediatrics|September 9, 2008
Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritanceG Eda Utine, Yasemin Alanay, Dilek Aktaş, et al.
Chest|September 16, 2005
Childhood parapneumonic effusions: biochemical and inflammatory markersG Eda Utine, Ugur Ozcelik, Ebru Yalcin, et al.
Journal of Child Neurology|April 25, 2013
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophyG Eda Utine, Göknur Haliloğlu, Bilge Salanci, et al.
Respiration; International Review of Thoracic Diseases|August 31, 2007
Pleural fluid PCR method for detection of Staphylococcus aureus, Streptococcus pneumoniae and Haemophilus influenzae in pediatric parapneumonic effusionsG Eda Utine, Ahmet Pinar, Uğur Ozçelik, et al.
European Journal of Medical Genetics|March 22, 2017
HERC1 mutations in idiopathic intellectual disabilityG Eda Utine, Ekim Z Taşkıran, Can Koşukcu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 11, 2014
Etiological yield of SNP microarrays in idiopathic intellectual disabilityG Eda Utine, Göknur Haliloğlu, Bilge Volkan-Salancı, et al.
The Turkish Journal of Pediatrics|October 13, 2009
Pediatric pleural effusions: etiological evaluation in 492 patients over 29 yearsG Eda Utine, Uğur Ozçelik, Nural Kiper, et al.
American Journal of Human Genetics|April 6, 2010
Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfectaYasemin Alanay, Hrispima Avaygan, Natalia Camacho, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individualsNuria Garcia Segarra, Laureane Mittaz, Ana Belinda Campos-Xavier, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
European Journal of Medical Genetics|February 14, 2006
Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogueG Eda Utine, Ayfer Alikasifoglu, Mehmet Alikasifoglu, et al.
The Turkish Journal of Pediatrics|September 9, 2008
Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritanceG Eda Utine, Yasemin Alanay, Dilek Aktaş, et al.
Chest|September 16, 2005
Childhood parapneumonic effusions: biochemical and inflammatory markersG Eda Utine, Ugur Ozcelik, Ebru Yalcin, et al.
Journal of Child Neurology|April 25, 2013
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophyG Eda Utine, Göknur Haliloğlu, Bilge Salanci, et al.
Respiration; International Review of Thoracic Diseases|August 31, 2007
Pleural fluid PCR method for detection of Staphylococcus aureus, Streptococcus pneumoniae and Haemophilus influenzae in pediatric parapneumonic effusionsG Eda Utine, Ahmet Pinar, Uğur Ozçelik, et al.
European Journal of Medical Genetics|March 22, 2017
HERC1 mutations in idiopathic intellectual disabilityG Eda Utine, Ekim Z Taşkıran, Can Koşukcu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 11, 2014
Etiological yield of SNP microarrays in idiopathic intellectual disabilityG Eda Utine, Göknur Haliloğlu, Bilge Volkan-Salancı, et al.
The Turkish Journal of Pediatrics|October 13, 2009
Pediatric pleural effusions: etiological evaluation in 492 patients over 29 yearsG Eda Utine, Uğur Ozçelik, Nural Kiper, et al.
American Journal of Human Genetics|April 6, 2010
Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfectaYasemin Alanay, Hrispima Avaygan, Natalia Camacho, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individualsNuria Garcia Segarra, Laureane Mittaz, Ana Belinda Campos-Xavier, et al.
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