Haploinsufficiency of ALX4 as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene-Deletion Syndrome.

Authors :: Yuan-Qing Wu
Badano, Jose L.
McCaskill, Christopher
Vogel, Hannes
Potocki, Lorraine
Shaffer, Lisa G.
Source :: American Journal of Human Genetics. Nov2000, Vol. 67 Issue 5. 6 Diagrams, 1 Chart.
Publication Year :: 2000
Abstract: Investigates the role of ALX4 in the mechanism of parietal foramina in contiguous gene-deletion syndrome. Presence of a deletion in the short arm of chromosome 11; Identification of chromosomal clone mapping from chromosome 11; Clinical characteristics of Potocki-Schaffer syndrome.

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