Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1

Muhammad Farooq, Shahid Baig, Niels Tommerup, Klaus W Kjaer

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

18 Citationer (Scopus)

Abstract

Udgivelsesdato: 2010-Feb
OriginalsprogEngelsk
TidsskriftAmerican Journal of Medical Genetics. Part A
Vol/bind152A
Udgave nummer2
Sider (fra-til)495-7
Antal sider2
ISSN1552-4825
DOI
StatusUdgivet - 2010

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