A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

scientific article

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0092-8674(93)90379-5
P3181OpenCitations bibliographic resource ID3253403
P698PubMed publication ID8106171
P5875ResearchGate publication ID15093423

P50authorEthylin Wang JabsQ16226714
P2093author name stringW Luo
M L Warman
X Li
I Klisak
L Ma
U Müller
J B Mulliken
R Sparkes
I S Haworth
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectcraniosynostosisQ378183
P304page(s)443-450
P577publication date1993-11-01
P1433published inCellQ655814
P1476titleA mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
P478volume75