Silver‐like syndrome and a small deletion on chromosome 13
Author:
Affiliation:
1. Department of Clinical Genetics, East Hospital, Gothenburg
2. Department of Clinical Genetics, University of Umeå
3. Department of Pediatrics, East Hospital, Gothenburg
4. Department of Pediatrics, University of Umeå, Sweden
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1651-2227.1993.tb12618.x
Reference13 articles.
1. DELETION SHORT ARM 18 AND SILVER-RUSSELL SYNDROME
2. Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromes.
3. An improved technique for chromosome preparations from human lymphocytes
4. A case of trisomy-G with a simultaneous balanced D-D translocation
Cited by 5 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. Response to Dr. H. Rivera regarding article “21 Mb deletion in chromosome band 13q22.2-q32.1 associated with mild/moderate psychomotor retardation, growth hormone insufficiency, short neck, micrognathia, hypotonia, dysplastic ears and other dysmorphic features”;European Journal of Medical Genetics;2011-07
2. Letter regarding the article: “21 Mb deletion in chromosome band 13q22.2–q32.1 associated with mild/moderate psychomotor retardation, growth hormone insufficiency, short neck, micrognathia, hypotonia, dysplastic ears and other dysmorphic features” by Grigori et al.;European Journal of Medical Genetics;2011-07
3. Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients;Journal of Medical Genetics;2009-09-14
4. S;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
5. Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3;American Journal of Medical Genetics Part A;2005
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