Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt-Reference-Cited by-同舟云学术

Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt

Published:2018-10-31 Issue:12 Volume:176 Page:2604-2613
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Čaplovičová Martina¹^ORCID,Moslerová Veronika¹²,Dupej Ján¹³,Macek Milan²,Zemková Dana²,Hoffmannová Eva¹,Havlovicová Markéta²,Velemínská Jana¹

Affiliation:

1. Department of Anthropology and Human Genetics, Faculty of Science; Charles University; Prague 2 Czech Republic

2. Department of Biology and Medical Genetics, 2nd Faculty of Medicine; Charles University and Motol University Hospital; Prague 5 Czech Republic

3. Department of Software and Computer Science, Faculty of Mathematics and Physics; Charles University; Prague 2 Czech Republic

Funder

2nd Faculty of Medicine, Charles University

Fakultní Nemocnice Motol

Grantová Agentura, Univerzita Karlova

Norway Grants

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40659/fullpdf

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4. Noonan syndrome: The changing phenotype;Allanson;American Journal of Medical Genetics,1985

5. Recent advances in RASopathies;Aoki;Journal of Human Genetics,2016

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