Prader-Willi-like phenotype in fragile X syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04018.x/fullpdf
Reference23 articles.
1. Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes;Beemer;Am J Med Genet,1986
2. Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients;Borghgraef;Clin Genet,1987
3. Do some patients with fragile X syndrome have precocious puberty;Butler;Am J Med Genet,1988
4. Prader-Willi syndrome: current understanding of cause and diagnosis;Butler;Am J Med Genet,1990
5. Relationship between diabetes mellitus and obesity in the child;Drash;Metabolism,1973
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2. The Spectrum of the Prader–Willi-like Pheno- and Genotype: A Review of the Literature;Endocrine Reviews;2021-08-30
3. FMRP-absence-induced up-regulation of hypothalamic MAP1B expression decreases AgRP level linking with reduces in food intake and body weight;Neurochemistry International;2020-11
4. Loss of Drosophila FMRP leads to alterations in energy metabolism and mitochondrial function;Human Molecular Genetics;2017-11-02
5. FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome;Clinical Case Reports;2017-03-23
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