Post-Zygotic Origin of Complete Maternal Chromosome 7 Isodisomy and Consequent Loss of Placental PEG1/MEST Expression-Reference-Cited by-同舟云学术

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Post-Zygotic Origin of Complete Maternal Chromosome 7 Isodisomy and Consequent Loss of Placental PEG1/MEST Expression

Published:2001-11 Issue:10 Volume:22 Page:813-821
ISSN:0143-4004
Container-title:Placenta
language:en
Short-container-title:Placenta

Author:

Miozzo M.,Grati F.R.,Bulfamante G.,Rossella F.,Cribiù M.,Radaelli T.,Cassani B.,Persico T.,Cetin I.,Pardi G.,Simoni G.

Publisher

Elsevier BV

Subject

Developmental Biology,Obstetrics and Gynecology,Reproductive Medicine

Reference25 articles.

1. Clinical and molecular findings in two patients with Silver-Russell syndrome and UPD 7: comparison with non-UPD 7 cases;Bernard;Am J Med Genet,1999

2. Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion;Blagitko;Hum Mol Genet,2000

3. Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy;Eggermann;Hum Genet,1997

4. A new genetic concept: uniparental disomy and its potential effect, isodisomy;Engel;Am J Med Genet,1980

5. Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas;Grati;Cancer Genet Cytogenet,2000

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1. Low-level mosaic trisomy 7 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 7 cell line and a favorable fetal outcome;Taiwanese Journal of Obstetrics and Gynecology;2024-07

2. Chromosome 7 Isodisomy in a Child with Silver-Russell Síndrome;OBM Genetics;2024-06-24

3. Genetic counseling of non-invasive prenatal testing (NIPT) trisomy 7-positive pregnancies;Taiwanese Journal of Obstetrics and Gynecology;2024-05

4. Extensive Placental Methylation Profiling in Normal Pregnancies;International Journal of Molecular Sciences;2021-02-21

5. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2020-01

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