Severe craniosynostosis in an infant with deletion 22q11.2 syndrome.

Al-Hertani, W; Hastings, V A; McGowan-Jordan, J; Hurteau, J; Graham, Gail E

Al-Hertani, W; Hastings, V A; McGowan-Jordan, J; Hurteau, J; Graham, Gail E.

Affiliation

Al-Hertani W; Department of Genetics, University of Ottawa, Ottawa, Ontario, Canada.

Am J Med Genet A ; 161A(1): 153-7, 2013 Jan.

Article in En | MEDLINE | ID: mdl-23239640

Subject(s)

Craniosynostoses/diagnosis; Craniosynostoses/genetics; DiGeorge Syndrome/genetics; Chromosomes, Human, Pair 22/genetics; Humans; Image Processing, Computer-Assisted; Infant; Karyotype; Male; Microarray Analysis; Mutation; Nuclear Proteins/genetics; Phenotype; Polymorphism, Single Nucleotide; Receptor, Fibroblast Growth Factor, Type 2/genetics; Receptor, Fibroblast Growth Factor, Type 3/genetics; Sequence Analysis, DNA; Twist-Related Protein 1/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Craniosynostoses / DiGeorge Syndrome Limits: Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2013 Type: Article Affiliation country: Canada

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