Prenatal diagnosis of trisomy 1q21-qter: Case report and review of literature

American Journal of Medical Genetics

Volumn 134 A, Issue 2, 2005, Pages 207-211

  Machlitt, Andrea ^a   Kuepferling, Peter ^b   Bommer, Christiane ^a   Koerner, Hannelore ^a   Chaoui, Rabih ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

^b Practice of Human Genetics   (Germany)

Author keywords

Cardiac defect; Chromosome 1; Prenatal diagnosis; Trisomy 1q; Urethral obstruction

Indexed keywords

ADULT; AMNIOTIC FLUID CELL; AUTOPSY; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME 1; CHROMOSOME 1Q; CHROMOSOME DUPLICATION; CLINICAL FEATURE; CONGENITAL HEART DISEASE; CRANIOFACIAL MALFORMATION; CYTOGENETICS; DUODENUM ATRESIA; FEMALE; FETUS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GESTATIONAL AGE; HAND MALFORMATION; HEART VENTRICLE HYPERTROPHY; HUMAN; HUMAN TISSUE; KARYOTYPE; MULTIPLE MALFORMATION SYNDROME; OMPHALOCELE; PHENOTYPE; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RARE DISEASE; REVIEW; SECOND TRIMESTER PREGNANCY; TRISOMY; URETHRA OBSTRUCTION;

CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GESTATIONAL AGE; HUMANS; KARYOTYPING; MALE; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY;

EID: 15944385268     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30588     Document Type: Review

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