Behavioral and cognitive functioning in individuals with Cantú syndrome-Reference-Cited by-同舟云学术

Behavioral and cognitive functioning in individuals with Cantú syndrome

Published:2021-05-30 Issue:8 Volume:185 Page:2434-2444
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Roessler Helen I.¹^ORCID,Heuvel Lieke M.²,Shields Kathleen³,Guilliams Kristin P.⁴⁵,Knoers Nine V. A. M.⁶,Haaften Gijs¹,Grange Dorothy K.³⁷,Haelst Mieke M.²⁸

Affiliation:

1. Department of Genetics, Center for Molecular Medicine University Medical Center Utrecht, Utrecht University Utrecht The Netherlands

2. Department of Clinical Genetics Amsterdam University Medical Centers Amsterdam The Netherlands

3. Division of Genetics and Genomic Medicine, Department of Pediatrics Washington University School of Medicine St. Louis Missouri USA

4. Division of Pediatric Neurology, Department of Neurology Washington University School of Medicine St. Louis Missouri USA

5. Division of Pediatric Critical Care, Department of Pediatrics Washington University School of Medicine St. Louis Missouri USA

6. Department of Genetics University Medical Center Groningen Groningen The Netherlands

7. Center for the Investigation of Membrane Excitability Diseases (CIMED) St. Louis Missouri USA

8. Department of Clinical Genetics VU Medical Center, Amsterdam University Medical Centers Amsterdam The Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62348

Reference29 articles.

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2. Achenbach T. &Rescorla L.(2003).Manual for the ASEBA Adult Forms & Profiles. Burlington VT: University of Vermont Research Center for Children Youth & Families (Dutch translation: Verhulst FC & van de Ende J. Erasmus MS—Sophia Kinderziekenhuis Postbus 2060 3000 CB Rotterdam www.aseba.nl).

3. Heritability of attention‐deficit hyperactivity disorder in adults

4. Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities – Support for the role of K(ATP) channels in this condition

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