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Ercan Mihci

Showing results (11-20 of 44) with videos related to

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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 24, 2007
Prenatal diagnosis and early treatment of fetal goitrous hypothyroidism and treatment results with two-year follow-upMehmet Simsek, Inanc Mendilcioglu, Ercan Mihci, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
A novel AXIN2 gene mutation in sagittal synostosisElanur Yilmaz, Ercan Mihci, Banu Guzel Nur, et al.
Clinical Dysmorphology|May 29, 2009
The phenotypic spectrum of trisomy 2: report of two new casesErcan Mihci, Gopalrao V N Velagaleti, Regina Ensenauer, et al.
Pediatric Neurology|August 19, 2019
Recent Advances in CraniosynostosisElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Environmental and Molecular Mutagenesis|July 14, 2009
Neutrophil oxidative metabolism in Down syndrome patients with congenital heart defectsOzlem Akinci, Ercan Mihci, Sukran Tacoy, et al.
Journal of Neurosurgery|May 1, 2007
Primary atypical teratoid/rhabdoid tumor of the clival region. Case reportSaim Kazan, Ethem Göksu, Ercan Mihci, et al.
European Journal of Medical Genetics|February 17, 2015
Chanarin-Dorfman syndrome: Genotype-Phenotype CorrelationBanu Guzel Nur, Pinar Gencpinar, Ayse Yuzbasıoglu, et al.
Gene|December 25, 2012
A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangementZafer Cetin, Sezin Yakut, Ozden Altiok Clark, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12Zafer Cetin, Ercan Mihci, Sezin Yakut, et al.
Gene|July 26, 2012
A patient with Down syndrome with a de novo derivative chromosome 21Zafer Cetin, Sezin Yakut, Ercan Mihci, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 24, 2007
Prenatal diagnosis and early treatment of fetal goitrous hypothyroidism and treatment results with two-year follow-upMehmet Simsek, Inanc Mendilcioglu, Ercan Mihci, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
A novel AXIN2 gene mutation in sagittal synostosisElanur Yilmaz, Ercan Mihci, Banu Guzel Nur, et al.
Clinical Dysmorphology|May 29, 2009
The phenotypic spectrum of trisomy 2: report of two new casesErcan Mihci, Gopalrao V N Velagaleti, Regina Ensenauer, et al.
Pediatric Neurology|August 19, 2019
Recent Advances in CraniosynostosisElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Environmental and Molecular Mutagenesis|July 14, 2009
Neutrophil oxidative metabolism in Down syndrome patients with congenital heart defectsOzlem Akinci, Ercan Mihci, Sukran Tacoy, et al.
Journal of Neurosurgery|May 1, 2007
Primary atypical teratoid/rhabdoid tumor of the clival region. Case reportSaim Kazan, Ethem Göksu, Ercan Mihci, et al.
European Journal of Medical Genetics|February 17, 2015
Chanarin-Dorfman syndrome: Genotype-Phenotype CorrelationBanu Guzel Nur, Pinar Gencpinar, Ayse Yuzbasıoglu, et al.
Gene|December 25, 2012
A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangementZafer Cetin, Sezin Yakut, Ozden Altiok Clark, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12Zafer Cetin, Ercan Mihci, Sezin Yakut, et al.
Gene|July 26, 2012
A patient with Down syndrome with a de novo derivative chromosome 21Zafer Cetin, Sezin Yakut, Ercan Mihci, et al.
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