Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: Report of two cases and review of the literature-Reference-Cited by-同舟云学术

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Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: Report of two cases and review of the literature

Published:2009-03 Issue:1 Volume:49 Page:8-14
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:

Author:

Yamamoto Kayono,Yoshihashi Hiroshi,Furuya Noritaka,Adachi Masanori,Ito Susumu,Tanaka Yukichi,Masuno Mitsuo,Chiyo Hideaki,Kurosawa Kenji

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1741-4520.2008.00212.x/fullpdf

Reference24 articles.

1. Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome;Boonen;Am J Med Genet,2005

2. Perinatal findings and molecular cytogenetic analysis of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome;Chen;Prenat Diagn,2006

3. The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma;Evans;Br J Cancer,1991

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

Cited by 32 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. 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

2. An investigation of metabolic disturbances, including urinary stone disease, hypothyroidism, and osteoporosis in basal cell nevus syndrome;Pediatric Dermatology;2022-05-16

3. Gorlin-goltz syndrome;Journal of Datta Meghe Institute of Medical Sciences University;2022

4. Microsomic and macrosomic body structure in children and adolescents affected by syndromes or diseases associated with neurodysfunction;Scientific Reports;2021-03-18

5. A familial case of overgrowth syndrome caused by a 9q22.3 microdeletion in a mother and daughter;European Journal of Medical Genetics;2020-05

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