El estudio cromosómico y la técnica de hibridación in situ con fluorescencia (FISH) en el diagnóstico de sindromes de microdeleción / Chromosome studies and fluorescence in situ hybridization (FISH) for the diagnosis of microdeletion syndromes
Med. infant
;
19(2,n.esp): 137-143, jun. 2012. tab, ilus
Article
in Spanish
| LILACS
| ID: lil-774304
Subject(s)
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Prader-Willi Syndrome
/
Chromosome Aberrations
/
Chromosome Deletion
/
Kallmann Syndrome
/
In Situ Hybridization, Fluorescence
/
Angelman Syndrome
/
Williams Syndrome
/
Diagnosis
/
Classical Lissencephalies and Subcortical Band Heterotopias
/
Smith-Magenis Syndrome
Type of study:
Diagnostic study
Limits:
Female
/
Humans
/
Male
/
Infant, Newborn
Language:
Spanish
Journal:
Med. infant
Journal subject:
Pediatrics
Year:
2012
Type:
Article
Affiliation country:
Argentina
Institution/Affiliation country:
Hospital de Pediatría Juan P. Garrahan/AR
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