Partial and complete trisomy 14 mosaicism: Clinical follow-up, cytogenetic and molecular analysis

Molecular Cytogenetics

Volumn 7, Issue 1, 2014, Pages

  Salas Labadía, Consuelo ^a   Lieberman, Esther ^a   Cruz Alcívar, Roberto ^a   Navarrete Meneses, Pilar ^a   Gómez, Samuel ^a   Cantú Reyna, Consuelo ^b   Buiting, Karin ^c   Durán McKinster, Carola ^a   Pérez Vera, Patricia ^a  

^a INSTITUTO NACIONAL DE PEDIATRÍA   (Mexico)

^b Genomi k S A P I de C V   (Mexico)

^c UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

Deletion 14q11.2; Marker chromosome 14; Microarray analysis; Trisomy 14 mosaicism

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 14; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; CLEFT PALATE; CLINICAL FEATURE; CONDUCTION DEAFNESS; FACE ASYMMETRY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HUMAN; HUMAN CELL; KARYOTYPE 47,XXX; MARKER CHROMOSOME; MENTAL DEFICIENCY; MICROARRAY ANALYSIS; MICROSATELLITE MARKER; NOCTURNAL ENURESIS; PARTIAL TRISOMY; PERIPHERAL LYMPHOCYTE; SHORT STATURE; TRISOMY; TRISOMY 14 MOSAICISM;

EID: 84908120494     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/s13039-014-0065-8     Document Type: Article

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