Molecular cytogenetic characterization of an inherited maternal duplication 20p11.21p13 associated with a small 20p11.21 deletion

American Journal of Medical Genetics, Part A

Volumn 152 A, Issue 12, 2010, Pages 3197-3202

  D'Angelo, Carla S ^a   De Oliveira, Mariana A ^a   De Castro, Claudia I E ^a   Koiffmann, Celia P ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

FLUOXETINE;

ADULT; AGGRESSIVENESS; CASE REPORT; CHROMOSOME 20P; CHROMOSOME 21P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL FEATURE; DEPRESSION; EXTRACHROMOSOMAL INHERITANCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MAPPING; HUMAN; LETTER; MOSAICISM; MOTOR DYSFUNCTION; PRIORITY JOURNAL; SCOLIOSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TRISOMY; X RAY;

CELLS, CULTURED; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOMES, HUMAN, PAIR 20; CYTOGENETIC ANALYSIS; DEVELOPMENTAL DISABILITIES; DNA COPY NUMBER VARIATIONS; FEMALE; HUMANS; LYMPHOCYTES; METAPHASE; MOSAICISM; MOTHERS; POLYMORPHISM, SINGLE NUCLEOTIDE; TRISOMY; YOUNG ADULT;

EID: 78649651496     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33741     Document Type: Letter

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