Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis-Reference-Cited by-同舟云学术

Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis

Published:2014-01-08 Issue:1 Volume:14 Page:
ISSN:1472-6823
Container-title:BMC Endocrine Disorders
language:en
Short-container-title:BMC Endocr Disord

Author:

Stagi Stefano,Lapi Elisabetta,Seminara Salvatore,Guarducci Silvia,Pantaleo Marilena,Giglio Sabrina,Chiarelli Francesco,de Martino Maurizio

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/article/10.1186/1472-6823-14-3/fulltext.html

Reference35 articles.

1. Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM: Phenotypic and cytogenetic spectrum of 9p trisomy. Genet Couns. 2007, 18: 29-48.

2. Rethoré MO, Larget-Piet L, Abonyi D, Boeswillwald M, Berger R, Carpentier S, Cruveiller J, Dutrillau B, Lafourcade J, Penneau M, Lejeune J: Sur quatre cas de trisomie pour le bras court du chromosome 9: individualisation d’une nouvelle entite morbide. Ann Genet. 1970, 13: 217-232.

3. Huret JL, Leonard C, Forestier B, Rethore MO, Lejeune J: Eleven new cases of del(9p) and features from 80 cases. J Med Genet. 1988, 25: 741-749. 10.1136/jmg.25.11.741.

4. Seghezzi L, Maraschio P, Bozzola M, Maserati E, Tupler R, Marchi A, Tiepolo L: Ring chromosome 9 with a 9p22.3-p24.3 duplication. Eur J Pediatr. 1999, 158: 791-793. 10.1007/s004310051206.

5. Schinzel A: Catalogue of unbalanced chromosome aberrations in man. 2001, New York: W de Gruyter Berlin, 2

Cited by 14 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. A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations;Chromosome Research;2024-03-19

2. A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations;2023-12-13

3. A de novo chromosome 9p duplication in a female child with short stature and developmental delay;SAGE Open Medical Case Reports;2023-01

4. Disorders of IGFs and IGF-1R signaling pathways;Molecular and Cellular Endocrinology;2020-12

5. Partial trisomy 9p and 14q microduplication in a patient with growth retardation: a case report and review of the literature;Journal of Pediatric Endocrinology and Metabolism;2020-03-26