A 4-Mb critical region for intrauterine growth retardation at 15q26
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.620416.x/fullpdf
Reference14 articles.
1. Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome;Tamura;Clin Dysmorphol,1993
2. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q;Kato;Am J Med Genet,2001
3. Postnatal overgrowth by 15q-trisomy and IUGR by 15q-monosomy due to familial translocation t (13;15): Dosage effect of IGF1R?;Nagai;Am J Med Genet
4. An infant with deletion of the distal long arm of chromosome 15 (q26.1-qter) and loss of insulin-like growth factor 1 receptor gene;Roback;Am J Med Genet,1991
5. The insulin-like growth factor 1 receptor gene is normally biallelically expressed in human juvenile tissue and tumours;Howard;Hum Mol Genet,1993
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. Review and hypothesis: Syndromes with severe intrauterine growth restriction and very short stature-Are they related to the epigenetic mechanism(s) of fetal survival involved in the developmental origins of adult health and disease?;American Journal of Medical Genetics Part A;2010-02
2. Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH;Prenatal Diagnosis;2009-05-19
3. Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: Two patients and review of the literature;American Journal of Medical Genetics Part A;2007
4. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia;Prenatal Diagnosis;2007
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