Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects (Q24290691)

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English	Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects	scientific article

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scholarly article

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Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects (English)

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Haploinsufficiency

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GOA release 2020-03-11

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A Baxová

3

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Andrew Oliver Mungo Wilkie

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ORCID Public Data File 2021

author name string

L A Mavrogiannis

1

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I Antonopoulou

2

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S Kutílek

4

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C A Kim

5

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S M Sugayama

6

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A Salamanca

7

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S A Wall

8

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G M Morriss-Kay

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A O Wilkie

10

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language of work or name

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publication date

January 2001

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Nature Genetics

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27

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1

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17-8

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Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

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WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2).

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Foramina parietalia permagna: report of nine cases in one family

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Prenatal sonographic appearance of foramina parietalia permagna

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Alx-4: cDNA cloning and characterization of a novel paired-type homeodomain protein

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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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Consolidated OpenCitations Corpus – April 2017

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release_p757iwhx2ragdhr3aaabk4hgmu

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

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