IRS1 and GRB2 as members of the IGF signal transduction pathway are not associated with intrauterine growth retardation and Silver-Russell syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2001.590515.x/fullpdf
Reference14 articles.
1. Current concepts of fetal growth restriction: part I. Causes, classification, and pathophysiology;Lin;Obstet Gynecol,1998
2. Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients;Wollmann;Eur J Pediatr,1995
3. Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography other than 15;Kotzot;Am J Med Genet,1999
4. Second observation of Silver-Russell syndrome in a carrier of a reciprocal translocation with one breakpoint at site 17q25;Midro;Clin Genet,1993
5. Severe Silver-Russell syndrome and translocation (17;20)(q25;q13);Ramirez-Duenas;Clin Genet,1992
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1. Asociación entre el sistema IGF y PAPP-A en ateroesclerosis coronaria;Archivos de Cardiología de México;2016-04
2. Genetik des Silver-Russell-Syndroms;Monatsschrift Kinderheilkunde;2005-03
3. Lack of Association of Birth Size with Polymorphisms of Two Imprinted Genes, IGF2R and GRB10;Journal of Pediatric Endocrinology and Metabolism;2004-01
4. Characterization of Genomic Variants in CSH1 and GH2, Two Candidate Genes for Silver-Russell Syndrome in 17q24-q25;Genetic Testing;2003-09
5. Evidence from skewed X inactivation for trisomy mosaicism in Silver-Russell syndrome;European Journal of Human Genetics;2001-12
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