(Q52101906)

22 April 2018

title

A novel locus for parietal foramina maps to chromosome 4q21-q23. (English)

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22 April 2018

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4

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22 April 2018

author name string

Gang Chen

1

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22 April 2018

Desan Zhang

2

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22 April 2018

Guoying Feng

3

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22 April 2018

Lin He

5

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22 April 2018

publication date

7 August 2003

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22 April 2018

Journal of Human Genetics

published in

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22 April 2018

volume

48

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22 April 2018

issue

8

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22 April 2018

page(s)

420-424

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22 April 2018

https://scigraph.springernature.com/pub.10.1007/s10038-003-0050-2

exact match

0 references

cites work

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Symptomatic large parietal foramina

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Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome

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Alx4 binding to LEF-1 regulates N-CAM promoter activity

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Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

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Chromosomal localization of three human genes encoding bone morphogenetic protein receptors

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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

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Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

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Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease

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Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna

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Familial incidence of foramina parietalia permagna

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Hereditary cranium bifidum and symmetric parietal foramina are the same entity

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12 December 2020

10.1007/S10038-003-0050-2

Identifiers

DOI

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22 April 2018

PubMed ID

12905082

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22 April 2018