Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13

Prenatal Diagnosis

Volumn 26, Issue 3, 2006, Pages 273-276

  Trimborn, Marc ^a   Wegner, Rolf Dieter ^a,b   Tönnies, Holger ^a   Sarioglu, Nanette ^a   Albig, Matthias ^b   Neitzel, Heidemarie ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b Centre of Prenatal Diagnosis   (Germany)

Author keywords

CGH; FISH; Interstitial duplication; Molecular cytogenetics

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; ARTICLE; CASE REPORT; CHROMOSOME 16Q; CHROMOSOME ABERRATION; CHROMOSOME DUPLICATION; CHROMOSOME PAINTING; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC COUNSELING; HUMAN; MOLECULAR CLONING; NERVE CELL DIFFERENTIATION; OVARY DISEASE; PARTIAL TRISOMY; PARTIAL TRISOMY 16Q; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY 16;

ABNORMALITIES, MULTIPLE; ADULT; ARTERIES; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 16; FACE; FEMALE; FETAL DISEASES; HUMANS; MUTATION; OVARY; PREGNANCY; PRENATAL DIAGNOSIS; THYROID GLAND;

EID: 33645385634     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1396     Document Type: Article

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