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Trisomy 20 (Duplication 20)
- TRISOMY 20 MOSAICISM
- An abnormal fetus with trisomy 20 and trisomy 9 mosaicism
- Trisomy 20 is a primary chromosome aberration in desmoid tumors
- Chromosome Deletion Outreach, Inc.
- Trisomy, monosomy, ring chromosome 20p and genetic imprinting references
- Trisomy 20 mosaicism
- Trisomy 20p
- Amniotic fluid cell mosaicism for presumptive trisomy 20
- Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20
- "... trisomy 20 which usually has a favourable outcome ..."
- "An imprinting effect may also cause the clinical features of UPD2O since prenatally detected mosaic trisomy 20 does usually not affect the pregnancy outcome."
- Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development
- "Trisomy 20 is characterized by profound mental retardation, abnormally large mouth and tongue, minor abnormalities of the ears, and other skeletal defects."
- "Deep fibromatosis...Associated with trisomy 20"
- "Trisomy 20 Mosaicism Dilemma of Trisomy 20 Mosaicism Detected Prenatally: is it an innocent finding, Am Journal of Med Genetics 1998"
- Parents of a child with partial monsony-16 and trisomy-20 fight for the child's education
- Trisomy 20
- Prenatal diagnosis of mosaic trisomy 20 in New Zealand
- Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis
- Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature
- Prenatal diagnosis of trisomy 20 by chorionic villus sampling (CVS): a case report with long-term outcome
- Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20
- Non-mosaic trisomy 20 presenting at 21 weeks' gestation as a thoraco-abdominal mass
- Prenatal diagnosis of trisomy 20 mosaicism by maternal serum screening for Down syndrome
- Autosomal trisomy 20 (61,XX,+20) in a malformed bovine fetus
- Frequency of trisomy 20 in nonmalignant bronchial epithelium from lung cancer patients and cancer-free former uranium miners and smokers
- Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
- A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism
- Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues
- Trisomy 20 in a papillary urothelial carcinoma of the ureter
- Trisomy 20 characterizes a second group of desmoid tumors
- An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line
- Intrauterine growth retardation associated with a mosaic trisomy 20 limited to the placenta. A case report
- Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male
- Non-mosaic trisomy 20 in cultures of amniotic fluid from a fetus with serious congenital malformation
- Trisomy 20 mosaicism in amniotic cell culture. Genetic counselling during the prenatal diagnosis
- Clonal cytogenetic changes in atherosclerotic plaques including trisomy 20
- A revisit of trisomy 20 mosaicism in prenatal diagnosis--an overview of 103 cases
- Hepatoblastoma characterized by trisomy 20 and double minutes
- Trisomy 20q caused by der (X)t(X;20)(q28;q11.2)
- Confirmation of prenatally ascertained trisomy 20 mosaicism
- Trisomy 20 mosaicism identified prenatally and confirmed in foreskin fibroblasts
- Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus
- Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn
- Chromosome analyses from urinary sediment: postnatal confirmation of a prenatally diagnosed trisomy 20 mosaicism
- Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literature
- Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicism
- Trisomy 20 mosaicism in prenatal diagnosis--a review and update
- Prenatal diagnosis of trisomy 20 mosaicism indicating an extra embryonic origin
- Follow-up of infants with amniotic fluid trisomy 20 mosaicism
- Multiple congenital anomalies in a child born after prenatal diagnosis of trisomy 20 mosaicism
- Prenatal diagnosis of a true mosaic trisomy 20 substantiated by demonstration of a gene dosage effect for adenosine deaminase (ADA)
- Further examples of trisomy-20 mosaicism in amniotic cell cultures
- Prenatal diagnosis of trisomy 20 mosaicism indicating esophageal and rectal origin
- On the significance of true trisomy 20 mosaicism in amniotic fluid culture
- Trisomy 20 mosaicism
- Genetic counselling for trisomy 20 mosaicism in amniotic fluid cell cultures
- Trisomy 20 mosaicism in amniotic fluid cells
- Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0)
- Partial trisomy 20
- Importance of trisomy-20 mosaicism to prenatal diagnosis
- Trisomy 20p from maternal t(3;20) translocation
- Prenatal diagnosis of trisomy 20 mosaicism
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