Screening for subtelomeric rearrangements using automated fluorescent genotyping of microsatellite markers: A Lebanese study

European Journal of Medical Genetics

Volumn 49, Issue 2, 2006, Pages 117-126

  Delague, Valérie ^a   Souaid, Myrna ^a   Chouery, Eliane ^a   Depetris, Danielle ^b   Sanlaville, Damien ^c   Mattei, Marie Geneviève ^b   Mégarbané, André ^a,d  

^a SAINT JOSEPH UNIVERSITY   (Lebanon)

^b INSERM   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d Saint Joseph University   (France)

Author keywords

Malformations; Mental retardation; Monosomy 3p; Monosomy 6p; Monosomy 7p; Telomeres; Trisomy 5q

Indexed keywords

ARTICLE; CHROMOSOME 3P; CHROMOSOME 5Q; CHROMOSOME 6P; CHROMOSOME 7P; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CONTROLLED STUDY; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; LEBANON; MALE; MENTAL DEFICIENCY; MICROSATELLITE MARKER; TELOMERE;

CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; FEMALE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; LEBANON; MALE; MICROSATELLITE REPEATS; MONOSOMY; TELOMERE; TRISOMY;

EID: 33644870002     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.04.022     Document Type: Article

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