Localization of craniosynostosis Adelaide type to 4p16.

doi:10.1093/hmg/4.4.681

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Article

Localization of craniosynostosis Adelaide type to 4p16.

Human molecular genetics - 1 Apr 1995

Hollway G E, Phillips H A, Adès L C, Haan E A, Mulley J C

Abstract excerpt

Craniosynostosis Adelaide type is a rare autosomal dominant syndrome associated with digital abnormalities. Linkage mapping was carried out excluding allelism to Saethre-Chotzen syndrome at 7p21, craniosynostosis Boston type at 5q34-q35, Jackson-Weiss and Crouzon syndromes at 10q24-q25 and Pfeiff...

Topics

Chromosome Mapping
Chromosomes, Human, Pair 4
Craniosynostoses
Genes, Dominant
Homeodomain Proteins
Humans
MSX1 Transcription Factor
Phenotype
Receptors, Fibroblast Growth Factor
Transcription Factors

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