(Q34137531)

31 July 2017

title

Discriminating power of localized three-dimensional facial morphology (English)

1 reference

31 July 2017

19

Raoul Hennekam

0 references

Annette Karmiloff-Smith

8

object named as

Annette Karmiloff-Smith

1 reference

31 July 2017

Linda E Campbell

5

0 references

Kieran Murphy

object named as

Kieran C Murphy

10

0 references

Judith Allanson

3

object named as

Judith E Allanson

1 reference

31 July 2017

Peter Hammond

1

1 reference

31 July 2017

Tim J Hutton

2

1 reference

31 July 2017

Bernard Buxton

4

1 reference

31 July 2017

Jill Clayton-Smith

6

1 reference

31 July 2017

Dian Donnai

7

1 reference

31 July 2017

Kay Metcalfe

9

1 reference

31 July 2017

Michael Patton

11

1 reference

31 July 2017

Barbara Pober

12

1 reference

31 July 2017

Katrina Prescott

13

1 reference

31 July 2017

Pete Scambler

14

1 reference

31 July 2017

Adam Shaw

15

1 reference

31 July 2017

Ann C M Smith

16

1 reference

31 July 2017

Angela F Stevens

17

1 reference

31 July 2017

I Karen Temple

18

1 reference

31 July 2017

May Tassabehji

20

1 reference

31 July 2017

language of work or name

English

0 references

publication date

26 October 2005

1 reference

American Journal of Human Genetics

31 July 2017

published in

1 reference

31 July 2017

volume

77

1 reference

31 July 2017

issue

6

1 reference

31 July 2017

page(s)

999-1010

1 reference

Role of TBX1 in human del22q11.2 syndrome

31 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=1285182

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

The face of Smith-Magenis syndrome: a subjective and objective study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Rubinstein-Taybi syndrome: objective evaluation of craniofacial structure

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Sotos syndrome: evolution of facial phenotype subjective and objective assessment.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

The 1993-94 Généthon human genetic linkage map

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Noonan syndrome: the changing phenotype.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Natural history of Williams syndrome: physical characteristics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

3D analysis of facial morphology.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Computer-based recognition of dysmorphic faces.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Estimating average growth trajectories in shape-space using kernel smoothing.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Mutations in RAI1 associated with Smith-Magenis syndrome.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Description of a dinucleotide repeat polymorphism in the human elastin gene and its use to confirm assignment of the gene to chromosome 7.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285182

Quantitative approach to identifying abnormal variation in the human face exemplified by a study of 278 individuals with five craniofacial syndromes

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16380911

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Photoanthropometric study of facial growth in Noonan syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16380911

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Anthropometric craniofacial pattern profiles in Down syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16380911

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/498396

1 reference

31 July 2017

1 reference

31 July 2017

1 reference