Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient

Genetic Counseling

Volumn 18, Issue 2, 2007, Pages 171-177

  Utine, Güllen Eda ^a   Aktas D ^a   Boduroglu K ^a   Alikasifoglu M ^a   Tuncbilek E ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Autosomal mosaicism; Fragile X syndrome; Monosomy 21

Indexed keywords

ANEUPLOIDY; ARTICLE; ATTENTION DISTURBANCE; CASE REPORT; CHILD; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; FACE DYSMORPHIA; FRAGILE X SYNDROME; HAND MOVEMENT; HUMAN; HYPERACTIVITY; MALE; MENTAL DEFICIENCY; MONOSOMY; MONOSOMY 21; MOSAICISM; MOTOR DEVELOPMENT; PHYSICAL EXAMINATION; SOCIAL ADAPTATION;

CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 21; COMORBIDITY; CRANIOFACIAL ABNORMALITIES; FACIES; FRAGILE X SYNDROME; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; MONOSOMY; MOSAICISM; PHENOTYPE;

EID: 34547162403     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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