Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype-Reference-Cited by-同舟云学术

Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype

Published:2013 Issue:1 Volume:14 Page:95
ISSN:1471-2156
Container-title:BMC Genetics
language:en
Short-container-title:BMC Genet

Author:

Bayrakli Fatih,Guclu Bulent,Yakicier Cengiz,Balaban Hatice,Kartal Ugur,Erguner Bekir,Sagiroglu Mahmut,Yuksel Sirin,Ozturk Ahmet,Kazanci Burak,Ozum Unal,Kars Hamit

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Embryology of the spine and associated congenital abnormalities

2. Sprengel Deformity: Pathogenesis and Management

3. The mechanism of somite formation in mice

4. Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the cranio-cervical joints of the axial skeleton

5. The concerted action of Meox homeobox genes is required upstream of genetic pathways essential for the formation, patterning and differentiation of somites

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