Trisomy 13 mosaicism in a phenotypically normal child: Description of cytogenetic and clinical findings from early pregnancy beyond 2 years of age'

American Journal of Medical Genetics, Part A

Volumn 143, Issue 5, 2007, Pages 518-520

  Di Giacomo, Marilena C ^a   Susca, Francesco C ^a   Resta, Nicoletta ^a   Bukvic, Nenad ^a   Vimercati, Antonella ^a   Guanti, Ginevra ^a,b  

^a UNIVERSITY OF BARI   (Italy)

^b POLICLINICO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; BLOOD CELL; CASE REPORT; CELL LINEAGE; CHEEK; CHROMOSOME ANALYSIS; CYTOGENETICS; FEMALE; FETUS; FIRST TRIMESTER PREGNANCY; GENETIC ASSOCIATION; GENETIC LINKAGE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN TISSUE; INFANT; KARYOTYPING; LETTER; MOSAICISM; PHENOTYPE; PREDICTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN FIBROBLAST; TRISOMY 13; URINARY TRACT;

CHILD DEVELOPMENT; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 13; CYTOGENETIC ANALYSIS; FEMALE; FETAL DEVELOPMENT; HUMANS; MOSAICISM; PHENOTYPE; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY;

EID: 33847371570     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31515     Document Type: Letter

References (7)

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