A familial interstitial 4q35 deletion with no discernible clinical effects-Reference-Cited by-同舟云学术

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A familial interstitial 4q35 deletion with no discernible clinical effects

Published:2015-04-05 Issue:8 Volume:167 Page:1836-1841
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Yakut Sezin¹,Clarck Ozden Altiok²,Sanhal Cem³,Nur Banu Guzel⁴,Mendilcioglu Inanc²,Karauzum Sibel Berker¹,Cetin Zafer⁵

Affiliation:

1. Department of Medical Biology and Genetics; Faculty of Medicine; Akdeniz University; Antalya Turkey

2. Department of Medical Genetics; Faculty of Medicine; Akdeniz University; Antalya Turkey

3. Department of Obstetrics and Gynaecology; Faculty of Medicine; Akdeniz University; Antalya Turkey

4. Department of Pediatric Genetics; Faculty of Medicine; Akdeniz University; Antalya Turkey

5. Department of Medical Biology; Faculty of Medicine; Sanko University; Gaziantep Turkey

Funder

Akdeniz University and Sanko University Scientific Research Project Management Foundations

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37097/fullpdf

Reference21 articles.

1. Phenotypic variability of a 4q34->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother;Bendavid;Eur J Med Genet,2007

2. Two newborns with chromosome 4 imbalances: Deletion 4q33->q35 and ring r(4)(pterq35.2-qter);Calabrese;Clin Genet,1997

3. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: Clinical description of a new patient;Caliebe;Clin Genet,1997

4. Identification and molecular characterization of two novel chromosomal deletions associated with autism;Chien;Clin Genet,2010

5. 4q35 deletion and 10p15 duplication associated with immunodeficiency;Cingoz;Am J Med Genet A,2006

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1. Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature;Cytogenetic and Genome Research;2024-08-01

2. Identification of a novel isolated 4q35.2 microdeletion in a Chinese pediatric patient using chromosomal microarray analysis: a case report and literature review;Molecular Cytogenetics;2023-08-02

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