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Ibrahim Vargel

Showing results (81-90 of 85) with videos related to

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Journal of Biomaterials Science. Polymer Edition|January 29, 2019
Critical-size alveolar defect treatment via TGF-ß3 and BMP-2 releasing hybrid constructsAybuke Alici-Garipcan, Petek Korkusuz, Elif Bilgic, et al.
American Journal of Human Genetics|May 11, 2010
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasiaElif Uz, Yasemin Alanay, Dilek Aktas, et al.
Human Molecular Genetics|August 21, 2009
ALX4 dysfunction disrupts craniofacial and epidermal developmentHulya Kayserili, Elif Uz, Carien Niessen, et al.
American Journal of Human Genetics|August 2, 2016
Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 SignalingArda Cetinkaya, Jingwei Rachel Xiong, İbrahim Vargel, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosisKatharina Keupp, Yun Li, Ibrahim Vargel, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
Journal of Biomaterials Science. Polymer Edition|January 29, 2019
Critical-size alveolar defect treatment via TGF-ß3 and BMP-2 releasing hybrid constructsAybuke Alici-Garipcan, Petek Korkusuz, Elif Bilgic, et al.
American Journal of Human Genetics|May 11, 2010
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasiaElif Uz, Yasemin Alanay, Dilek Aktas, et al.
Human Molecular Genetics|August 21, 2009
ALX4 dysfunction disrupts craniofacial and epidermal developmentHulya Kayserili, Elif Uz, Carien Niessen, et al.
American Journal of Human Genetics|August 2, 2016
Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 SignalingArda Cetinkaya, Jingwei Rachel Xiong, İbrahim Vargel, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosisKatharina Keupp, Yun Li, Ibrahim Vargel, et al.
Pageof 9