(Q33680617)

28 July 2017

title

Craniosynostosis and chromosome 22q11 deletion (English)

1 reference

28 July 2017

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Dean JC

1

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28 July 2017

De Silva DC

series ordinal

2

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28 July 2017

Reardon W

series ordinal

3

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28 July 2017

language of work or name

English

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publication date

1 April 1998

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

35

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28 July 2017

issue

4

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28 July 2017

page(s)

346; author reply 347

1 reference

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051294

Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051294

Cranial hemihypertrophy and neurodevelopmental prognosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051294

Family studies in chromosome 22q11 deletion: further demonstration of phenotypic heterogeneity.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051294

A population-based study of craniosynostosis

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051294

30 October 2018

Identifiers

DOI

10.1136/JMG.35.4.346

1 reference

28 July 2017

1 reference

28 July 2017

1 reference