Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions-Reference-Cited by-同舟云学术

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Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions

Published:2018-10-22 Issue:12 Volume:176 Page:2901-2906
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Dugan Sarah L.¹,Panza Emanuele²³,Openshaw Amanda⁴,Botto Lorenzo D.¹,Camacho Jose A.⁵,Toydemir Reha M.¹⁴⁶^ORCID

Affiliation:

1. Department of Pediatrics; University of Utah; Salt Lake City Utah

2. Department of Human Genetics; University of Utah; Salt Lake City Utah

3. Department of Medical and Surgical Sciences; University of Bologna; Italy

4. ARUP Laboratories; Salt Lake City Utah

5. Department of Pediatrics; Miller Children's and Women's Hospital; Long Beach California

6. Department of Pathology; University of Utah; Salt Lake City Utah

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40664/fullpdf

Reference16 articles.

1. Patients carrying 9q31.1-q32 deletion share common features with Cornelia de Lange syndrome;Cao;Cellular Physiology and Biochemistry,2015

2. A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1-9q33.1 deletion in a girl with a cleft lip and palate;Chien;American Journal of Medical Genetics Part A,2010

3. African American hypertensive nephropathy maps to a new locus on chromosome 9q31-q32;Chung;American Journal of Human Genetics,2003

4. Patients with deletions of 9q22q34 do not define a syndrome: Three case reports and a literature review;Farrell;Clinical Genetics,1991

5. Rare interstitial deletion 9q31.2 to q33.1 de novo: Longitudinal study in a patient over a period of more than 20 years;Gamerdinger;American Journal of Medical Genetics Part A,2008

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462;Molecular Genetics & Genomic Medicine;2022-12-03

2. Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate;Molecular Syndromology;2022-10-27

3. Pregnancy Outcome and Postnatal Chromosome Analysis of the Cord Blood and Chorionic Villi in Two Cases after Intrauterine Transfer of Mosaic Aneuploid Blastocysts;Case Reports in Obstetrics and Gynecology;2022-07-19

4. Kallmann syndrome in a patient with Weiss–Kruszka syndrome and a de novo deletion in 9q31.2;European Journal of Endocrinology;2021-07-01

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