Found: 25
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Risk of Fetal Loss in Pregnancies Undergoing Midtrimester Amniocentesis after Inconclusive Chorionic Villus Sampling.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Loss of heterozygosity on chromosome 4q32–35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes.
- Published in:
- Journal of Cutaneous Pathology, 2004, v. 31, n. 4, p. 318, doi. 10.1111/j.0303-6987.2004.0187.x
- By:
- Publication type:
- Article
Recombinant Chromosome 4 from a Familial Pericentric Inversion: Prenatal and Adulthood Wolf-Hirschhorn Phenotypes.
- Published in:
- Case Reports in Genetics, 2013, p. 1, doi. 10.1155/2013/306098
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- Publication type:
- Article
First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Risk of Fetal Loss in Pregnancies Undergoing Midtrimester Amniocentesis after Inconclusive Chorionic Villus Sampling.
- Published in:
- Fetal Diagnosis & Therapy, 2019, v. 46, n. 3, p. 149, doi. 10.1159/000493206
- By:
- Publication type:
- Article
Internalization of nanopolymeric tracers does not alter characteristics of placental cells.
- Published in:
- Journal of Cellular & Molecular Medicine, 2016, v. 20, n. 6, p. 1036, doi. 10.1111/jcmm.12820
- By:
- Publication type:
- Article
Patient experience with non-invasive prenatal testing (NIPT) as a primary screen for aneuploidy in the Netherlands.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study).
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1575, doi. 10.1002/pd.6271
- By:
- Publication type:
- Article
Confirmation rate of cell free DNA screening for sex chromosomal abnormalities according to the method of confirmatory testing.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1258, doi. 10.1002/pd.5814
- By:
- Publication type:
- Article
Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 652, doi. 10.1002/pd.5941
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- Publication type:
- Article
Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Obituary: Bruno Brambati, MD (29 February 1940-3 August 2020).
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Chromosomal mosaicism: Origins and clinical implications in preimplantation and prenatal diagnosis.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Aneuploidy in first trimester chorionic villi and spontaneous abortions: Windows into the origin and fate of aneuploidy through embryonic and fetal development.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Noninvasive screening by cell-free DNA for 22q11.2 deletion: Benefits, limitations, and challenges.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Comment on "The clinical utility of genome-wide non invasive prenatal screening".
- Published in:
- 2017
- By:
- Publication type:
- Letter
Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.
- Published in:
- 2015
- By:
- Publication type:
- journal article
The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
- Published in:
- Prenatal Diagnosis, 2015, v. 35, n. 8, p. 801, doi. 10.1002/pd.4613
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- Publication type:
- Article
Increased risk after noninvasive prenatal screening on cell-free DNA circulating in maternal blood: does a new indication for invasive prenatal diagnosis require new criteria for confirmatory cytogenetic analysis?
- Published in:
- 2015
- By:
- Publication type:
- Other
Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations.
- Published in:
- Prenatal Diagnosis, 2015, v. 35, n. 1, p. 35, doi. 10.1002/pd.4478
- By:
- Publication type:
- Article
De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.
- Published in:
- Prenatal Diagnosis, 2014, v. 34, n. 5, p. 460, doi. 10.1002/pd.4330
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- Publication type:
- Article
Prenatal diagnosis of del(4)(q27q31.23), due to a maternal balanced complex chromosome rearrangement, characterized by array-CGH.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 280, doi. 10.1002/pd.2439
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- Publication type:
- Article
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.
- Published in:
- Genes, 2023, v. 14, n. 1, p. 160, doi. 10.3390/genes14010160
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- Publication type:
- Article