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Ercan Mihci

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American Journal of Medical Genetics. Part A|August 2, 2008
Germline duplication of chromosomes 10p15.3 and Yp11.32 in a man with learning disability and early onset cutaneous malignant melanomaErcan Mihci, Noralane M Lindor
American Journal of Medical Genetics. Part A|April 29, 2008
DOOR (deafness, onychodystrophy, osteodystrophy, mental retardation) syndrome in one of the twins after conception with intracytoplasmic sperm injectionErcan Mihci, Kenan Guney, Sevtap Velipasaoglu
Journal of Bone and Mineral Metabolism|May 20, 2016
Bone mineral density in patients with mucopolysaccharidosis type IIIBanu Guzel Nur, Hakan Nur, Ercan Mihci
Indian Pediatrics|December 7, 2007
Oral-facial digital syndrome type 1Ercan Mihci, Sukran Tacoy, Gulay Ozbilim, et al.
Pediatric Surgery International|July 19, 2005
Currarino syndrome associated with penoscrotal inversion and perineal fissureAdnan Aslan, Güngör Karagüzel, Ercan Mihci, et al.
Prenatal Diagnosis|January 31, 2009
Prenatal diagnosis of Gollop-Wolfgang complex (tibial agenesis and femoral bifurcation)Inanc Mendilcioglu, Ercan Mihci, Elif Pestereli, et al.
American Journal of Medical Genetics. Part A|July 30, 2019
Coronal craniosynostosis due to TCF12 mutations in patients from TurkeyElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Fetal Diagnosis and Therapy|April 13, 2005
Evaluation of a fetus with Neu-Laxova syndrome through prenatal, clinical, and pathological findingsErcan Mihci, Mehmet Simsek, Inanc Mendilcioglu, et al.
The Journal of Dermatology|April 20, 2006
PHACES syndrome presenting as hemangiomas, sternal clefting and congenital ulcerations on the helicesCicek Durusoy, Ercan Mihci, Sukran Tacoy, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 geneErcan Mihci, Doğa Türkkahraman, Sian Ellard, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|August 2, 2008
Germline duplication of chromosomes 10p15.3 and Yp11.32 in a man with learning disability and early onset cutaneous malignant melanomaErcan Mihci, Noralane M Lindor
American Journal of Medical Genetics. Part A|April 29, 2008
DOOR (deafness, onychodystrophy, osteodystrophy, mental retardation) syndrome in one of the twins after conception with intracytoplasmic sperm injectionErcan Mihci, Kenan Guney, Sevtap Velipasaoglu
Journal of Bone and Mineral Metabolism|May 20, 2016
Bone mineral density in patients with mucopolysaccharidosis type IIIBanu Guzel Nur, Hakan Nur, Ercan Mihci
Indian Pediatrics|December 7, 2007
Oral-facial digital syndrome type 1Ercan Mihci, Sukran Tacoy, Gulay Ozbilim, et al.
Pediatric Surgery International|July 19, 2005
Currarino syndrome associated with penoscrotal inversion and perineal fissureAdnan Aslan, Güngör Karagüzel, Ercan Mihci, et al.
Prenatal Diagnosis|January 31, 2009
Prenatal diagnosis of Gollop-Wolfgang complex (tibial agenesis and femoral bifurcation)Inanc Mendilcioglu, Ercan Mihci, Elif Pestereli, et al.
American Journal of Medical Genetics. Part A|July 30, 2019
Coronal craniosynostosis due to TCF12 mutations in patients from TurkeyElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Fetal Diagnosis and Therapy|April 13, 2005
Evaluation of a fetus with Neu-Laxova syndrome through prenatal, clinical, and pathological findingsErcan Mihci, Mehmet Simsek, Inanc Mendilcioglu, et al.
The Journal of Dermatology|April 20, 2006
PHACES syndrome presenting as hemangiomas, sternal clefting and congenital ulcerations on the helicesCicek Durusoy, Ercan Mihci, Sukran Tacoy, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 geneErcan Mihci, Doğa Türkkahraman, Sian Ellard, et al.
Pageof 5