Management of the CNVs in constitutional human genetics using array CGH;Gestion des variations du nombre de séquences génomiques (CNV) en génétique humaine constitutionnelle utilisant l'hybridation génomique comparative en microréseau d'ADN (HGCM)

Pathologie Biologie

Volumn 56, Issue 6, 2008, Pages 354-361

  Nemos, C ^a   Bursztejn, A C ^a   Jonveaux, P ^a  

^a CHU NANCY BRABOIS   (France)

Author keywords

Array CGH; CNV; Constitutional; Genetics; Human

Indexed keywords

MICROSATELLITE DNA;

ANEUPLOIDY; ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DIAGNOSTIC PROCEDURE; DNA MICROARRAY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE INSERTION; GENETIC DISORDER; GENETIC VARIABILITY; GENETICS; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MICROSCOPY; TECHNOLOGY;

DATABASES, FACTUAL; DATABASES, GENETIC; GENE DOSAGE; GENETIC DISEASES, INBORN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MINISATELLITE REPEATS; MOLECULAR DIAGNOSTIC TECHNIQUES; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; OLIGONUCLEOTIDE PROBES; POLYMERASE CHAIN REACTION; QUALITY CONTROL; TERMINOLOGY AS TOPIC;

EID: 50949120651     PISSN: 03698114     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.patbio.2008.03.015     Document Type: Article

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