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WIREs Dev Biol

Birth Defects

Listings: 1-10   11-18
Morphogenetic movements in the neural plate and neural tube: mouse

Advanced Review
R'ada Massarwa, Heather J. Ray, Lee Niswander
Published Online: May 29 2013
DOI:10.1002/wdev.120

Abstract Full article on Wiley Online Library:   HTML | PDF
Cardiac outflow tract anomalies

Advanced Review
Zachary Neeb, Jacquelyn D. Lajiness, Esther Bolanis, Simon J Conway
Published Online: Feb 19 2013
DOI:10.1002/wdev.98

Abstract Full article on Wiley Online Library:   HTML | PDF
Birth defects associated with perturbations in preimplantation, gastrulation, and axis extension: from conjoined twinning to caudal dysgenesis

Overview
Anna Ferrer‐Vaquer, Anna‐Katerina Hadjantonakis
Published Online: Nov 26 2012
DOI:10.1002/wdev.97

Abstract Full article on Wiley Online Library:   HTML | PDF
Genetic causes of microcephaly and lessons for neuronal development

Advanced Review
Edward C. Gilmore, Christopher A. Walsh
Published Online: Oct 04 2012
DOI:10.1002/wdev.89

Abstract Full article on Wiley Online Library:   HTML | PDF
The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1

Focus Article
Irinna Papangeli, Peter Scambler
Published Online: Jun 19 2012
DOI:10.1002/wdev.75

Abstract Full article on Wiley Online Library:   HTML | PDF
Neural tube defects—disorders of neurulation and related embryonic processes

Advanced Review
Andrew J. Copp, Nicholas D. E. Greene
Published Online: May 29 2012
DOI:10.1002/wdev.71

Abstract Full article on Wiley Online Library:   HTML | PDF
Cytoskeleton in action: lissencephaly, a neuronal migration disorder

Focus Article
Hyang Mi Moon, Anthony Wynshaw‐Boris
Published Online: May 29 2012
DOI:10.1002/wdev.67

Abstract Full article on Wiley Online Library:   HTML | PDF
Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition

Advanced Review
Martyn T. Cobourne, Paul T. Sharpe
Published Online: May 25 2012
DOI:10.1002/wdev.66

Abstract Full article on Wiley Online Library:   HTML | PDF
The etiology and molecular genetics of human pigmentation disorders

Focus Article
Laura L. Baxter, William J. Pavan
Published Online: May 17 2012
DOI:10.1002/wdev.72

Abstract Full article on Wiley Online Library:   HTML | PDF
Rare syndromes of the head and face—Pierre Robin sequence

Focus Article
Tiong Yang Tan, Peter G. Farlie
Published Online: May 14 2012
DOI:10.1002/wdev.69

Abstract Full article on Wiley Online Library:   HTML | PDF

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In the Spotlight

Philip Benfey

Philip Benfey

Is intrigued by one of the key questions in developmental biology: how cells acquire their identities. This is an important question in human development, where stem cells divide and differentiate into skin, muscle, fat etc. It is equally central to plant development, where most organs and cells are formed from stem cell populations known as meristems. The Benfey lab addresses this question using a combination of genetics, molecular biology, and genomics to identify and characterize the genes that regulate formation of the root in the plant model system, Arabidopsis thaliana. The choice of the root as a model was based on the simplicity of its organization and its stereotyped developmental program.

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