Literature DB >> 4994115

[Lacunar changes in the parietal bones. Observations on 75 members of a family with an increased occurrece of parietal foramia].

E Schmidt-Wittkamp, H Christians.   

Abstract

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Year:  1970        PMID： 4994115

Source DB:  PubMed          Journal:  Fortschr Geb Rontgenstr Nuklearmed        ISSN： 0015-8151


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  2 in total

1.  Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Authors:  O Bartsch; W Wuyts; W Van Hul; J T Hecht; P Meinecke; D Hogue; W Werner; B Zabel; G K Hinkel; C M Powell; L G Shaffer; P J Willems
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

2.  Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.

Authors:  Lampros A Mavrogiannis; Indira B Taylor; Sally J Davies; Feliciano J Ramos; José L Olivares; Andrew O M Wilkie
Journal:  Eur J Hum Genet       Date:  2006-02       Impact factor: 4.246
  2 in total

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