(Q34311125)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25333067%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

title

Craniofacial morphometric analysis of individuals with X-linked hypohidrotic ectodermal dysplasia (English)

1 reference

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21 February 2020

4

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21 February 2020

Ophir D Klein

19

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21 February 2020

16

Richard A Spritz

1 reference

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21 February 2020

Benedikt Hallgrímsson

17

object named as

Benedikt Hallgrímsson

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21 February 2020

15

Dorothy K Grange

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21 February 2020

author name string

Alice F Goodwin

1

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21 February 2020

Jacinda R Larson

2

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21 February 2020

Kyle B Jones

3

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21 February 2020

Maya Landan

5

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21 February 2020

Zhifeng Wang

6

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21 February 2020

Anne Boekelheide

7

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21 February 2020

Margaret Langham

8

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21 February 2020

Vagan Mushegyan

9

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21 February 2020

Snehlata Oberoi

10

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21 February 2020

Rosalie Brao

11

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21 February 2020

Timothy Wen

12

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21 February 2020

Ramsey Johnson

13

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21 February 2020

Kenneth Huttner

14

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21 February 2020

Andrew H Jheon

18

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21 February 2020

language of work or name

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20 May 2014

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Molecular genetics & genomic medicine

21 February 2020

published in

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21 February 2020

volume

2

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21 February 2020

issue

5

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21 February 2020

page(s)

422-429

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Deciphering the Palimpsest: Studying the Relationship Between Morphological Integration and Phenotypic Covariation

21 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

Craniofacial characteristics of fragile X syndrome in mouse and man.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

MorphoJ: an integrated software package for geometric morphometrics

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

The Ectodysplasin and NFkappaB signalling pathways in odontogenesis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

Heterochrony and allometry: the analysis of evolutionary change in ontogeny.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4190877

3D analysis of facial morphology.

6 July 2018

1 reference

Analysis of craniofacial development in children with hypohidrotic ectodermal dysplasia.

21 January 2018

1 reference

Anthropometric and cephalometric measurements in X-linked hypohidrotic ectodermal dysplasia.

21 January 2018

1 reference

Molecular aspects of hypohidrotic ectodermal dysplasia.

21 January 2018

1 reference

X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings

21 January 2018

1 reference

The face signature of fibrodysplasia ossificans progressiva

21 January 2018

1 reference

12 December 2020

Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations

1 reference

12 December 2020

Facial morphometrics in the identification of gene carriers of X-linked hypohidrotic ectodermal dysplasia

1 reference

12 December 2020

Mutations in the EDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia

1 reference

12 December 2020

Identifiers

DOI

10.1002/MGG3.84

1 reference

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21 February 2020

1 reference

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21 February 2020

PubMed publication ID

25333067

1 reference

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