Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance
Open Access
- 15 October 2008
- journal article
- case report
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 17 (4) , 434-443
- https://doi.org/10.1038/ejhg.2008.192
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Different‐sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infectionsAmerican Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2008
- Filamin A and FILIP (Filamin A-Interacting Protein) Regulate Cell Polarity and Motility in Neocortical Subventricular and Intermediate Zones during Radial MigrationJournal of Neuroscience, 2004
- Functional disomy resulting from duplications of distal Xq in four unrelated patientsHuman Genetics, 2004
- Disomy of distal Xq in males: Case report and overviewAmerican Journal of Medical Genetics Part A, 2004
- Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplificationNucleic Acids Research, 2002
- Inherited duplication of Xq27.2 ??? qter: phenocopy of infantile Prader-Willi syndromeClinical Dysmorphology, 2001
- Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder.Journal of Medical Genetics, 1997
- The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28.1996
- Congenital intestinal pseudo-obstruction associated with a giant platelet disorderJournal of Medical Genetics, 1991
- Natal teeth, patent ductus arteriosus and intestinal pseudo‐obstruction: A lethal syndrome in the newbornClinical Genetics, 1976