Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4-Reference-Cited by-同舟云学术

Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

Published:2010-07 Issue:1 Volume:87 Page:40-51
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Guernsey Duane L.,Jiang Haiyan,Hussin Julie,Arnold Marc,Bouyakdan Khalil,Perry Scott,Babineau-Sturk Tina,Beis Jill,Dumas Nadine,Evans Susan C.,Ferguson Meghan,Matsuoka Makoto,Macgillivray Christine,Nightingale Mathew,Patry Lysanne,Rideout Andrea L.,Thomas Aidan,Orr Andrew,Hoffmann Ingrid,Michaud Jacques L.,Awadalla Philip,Meek David C.,Ludman Mark,Samuels Mark E.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference58 articles.

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2. Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation;Roberts;J. Med. Genet.,2002

3. Human microcephaly;Woods;Curr. Opin. Neurobiol.,2004

4. Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings;Woods;Am. J. Hum. Genet.,2005

5. Microcephaly syndromes;Abuelo;Semin. Pediatr. Neurol.,2007

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