Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): Further delineation of trisomies 1q

Fetal Diagnosis and Therapy

Volumn 16, Issue 5, 2001, Pages 265-273

  Bartsch, Christine ^a   Aslan, Mücevher ^a   Köhler, Jutta ^a   Miny, Peter ^b   Horst, Jürgen ^b   Holzgreve, Wolfgang ^c   Rehder, Helga ^a   Fritz, Barbara ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b UNIVERSITY OF MÜNSTER   (Germany)

^c UNIVERSITY WOMEN S HOSPITAL   (Switzerland)

Author keywords

Archived fetal tissues; Comparative genome hybridization; Dup (1q); Genotype phenotype correlations

Indexed keywords

FORMALDEHYDE; PARAFFIN;

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 1Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CHROMOSOME SIZE; CHROMOSOME STRUCTURE; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DISEASE COURSE; FEMALE; FETUS; FETUS DEATH; FETUS MALFORMATION; GENE ISOLATION; HUMAN; HUMAN TISSUE; INTELLECT; KARYOTYPE; LIFESPAN; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PARTIAL TRISOMY; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SURVIVAL TIME;

ADULT; AMNIOCENTESIS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENE DUPLICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; NUCLEIC ACID HYBRIDIZATION; PREGNANCY; TRISOMY;

EID: 0034885186     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000053926     Document Type: Article

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