Tremor is a major feature of 9p13 deletion syndrome-Reference-Cited by-同舟云学术

Tremor is a major feature of 9p13 deletion syndrome

Published:2020-09-08 Issue:11 Volume:182 Page:2694-2698
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Ferreira Susana Isabel¹,Cinnirella Giacomo²,Ramos Lina³,Suppa Antonio⁴⁵,Pires Luís Miguel¹,Nardone Anna Maria⁶,Camerota Letizia²,Lanciotti Silvia²,Galasso Cinzia⁷,De Maio Fernando⁸,Melo Joana Barbosa¹⁹¹⁰,Carreira Isabel Marques¹⁹¹⁰,Brancati Francesco¹¹¹²^ORCID

Affiliation:

1. Laboratory of Cytogenetics and Genomics, Faculty of Medicine University of Coimbra Coimbra Portugal

2. Medical Genetics Residency Program Tor Vergata University of Rome and University of L'Aquila L'Aquila Italy

3. Medical Genetics Unit Pediatric Hospital, Coimbra Hospital and University Centre Coimbra Portugal

4. Department of Human Neurosciences Sapienza University Rome Italy

5. Neuromed IRCCS Pozzilli Isernia Italy

6. Laboratory of Medical Genetics Policlinico Tor Vergata Rome Italy

7. Department of Systems Medicine, Division of Child Neurology and Psychiatry Tor Vergata University of Rome Rome Italy

8. Department of Orthopaedic Surgery Tor Vergata University of Rome Rome Italy

9. Coimbra Institute for Clinical and Biomedical Research (iCBR), Area of Environment, Genetics and Oncobiology (CIMAGO), Faculty of Medicine University of Coimbra, Center for Innovative Biomedicine and Biotechnology (CIBB) Coimbra Portugal

10. Clinical Academic Center of Coimbra (CACC) Coimbra Portugal

11. Medical Genetics Laboratory, Department of Life, Health and Environmental Sciences University of L'Aquila L'Aquila Italy

12. Istituto Dermopatico dell'Immacolata IDI‐IRCCS Rome Italy

Funder

Università degli Studi dell'Aquila

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61807

Reference7 articles.

1. 9p13.1p13.3 interstitial deletion: A case report and further delineation of a rare condition

2. Neurodevelopmental and Behavioral Abnormalities Associated With Deletion of Chromosome 9p

3. A case of de novo interstitial deletion of chromosome 9(p12p13)

4. Report of two patients and further characterization of interstitial 9p13 deletion-A rare but recurrent microdeletion syndrome?

5. Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype

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