| Cytogenetic evidence of involvement of chromosome regions 15q12 and 12q15 in conditions with associated overgrowth. | |
| | |
MedLine Citation:
|
PMID: 8466645 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
Syndromes with associated overgrowth are poorly understood. Besides their mode of inheritance, nothing is known regarding the basic genetic alterations that lead to their abnormal phenotypic manifestations. The chromosome localization of the genes involved remains unknown for this group of syndromes, with the only exception being the Wiedemann-Beckwith syndrome. |
| | |
Authors:
|
A Wajntal; D Moretti-Ferreira; D H De Souza; C P Koiffmann |
Related Documents
:
|
8178815 - Imprinting mutations suggested by abnormal dna methylation patterns in familial angelma... 15941405 - The chips domain--ancient traces for the hermansky-pudlak syndrome. 11907515 - A novel missense mutation of nsdhl in an unusual case of child syndrome showing bilater... 16937455 - Mutations of the aaas gene in an indian family with allgrove's syndrome. 22091325 - Pentalogy of cantrell: a report of three cases. 8178815 - Imprinting mutations suggested by abnormal dna methylation patterns in familial angelma... |
Publication Detail:
|
Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
|
Title: DNA and cell biology Volume: 12 ISSN: 1044-5498 ISO Abbreviation: DNA Cell Biol. Publication Date: 1993 Apr |
Date Detail:
|
Created Date: 1993-05-12 Completed Date: 1993-05-12 Revised Date: 2006-11-15 |
Medline Journal Info:
|
Nlm Unique ID: 9004522 Medline TA: DNA Cell Biol Country: UNITED STATES |
Other Details:
|
Languages: eng Pagination: 227-31 Citation Subset: IM |
Affiliation:
|
Department of Biology, University of São Paulo, Brazil. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Abnormalities, Multiple
/
genetics* Child, Preschool Chromosome Aberrations Chromosomes, Human, Pair 12* Chromosomes, Human, Pair 15* Female Growth Disorders / genetics* Humans Infant Karyotyping Male |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: 5' structure and expression of human glucose-6-phosphate dehydrogenase mRNA.
Next Document: Induction of O6-methylguanine-DNA-methyltransferase and N3-methyladenine-DNA-glycosylase in human ce...