Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype (Q24548200)

6

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author name string

Lampros A Mavrogiannis

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Indira B Taylor

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Sally J Davies

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José L Olivares

European Journal of Human Genetics

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language of work or name

English

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publication date

February 2006

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published in

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volume

14

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issue

2

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page(s)

151-8

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cites work

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Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2

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12 December 2020

Parietal foramina are not synonymous with giant parietal foramina

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12 December 2020

Foramina parietalia permagna

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12 December 2020

Hereditary enlarged parietal foramina (foramina parietalia permagna). Prenatal diagnosis, evolution and family study

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Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family

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Syndromic foramina parietalia permagna

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