Found: 31
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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
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- 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
Genetic diagnosis by chorionic villus sampling before 8 gestational weeks: Efficiency, reliability, and risks on 317 completed pregnancies.
- Published in:
- Prenatal Diagnosis, 1992, v. 12, n. 10, p. 789, doi. 10.1002/pd.1970121004
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- Publication type:
- Article
First-trimester genetic diagnosis in multiple pregnancy: Principles and potential pitfalls.
- Published in:
- Prenatal Diagnosis, 1991, v. 11, n. 10, p. 767, doi. 10.1002/pd.1970111005
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- Publication type:
- Article
Sister chromatid exchanges in first-trimester chorionic villi after in vivo and in vitro exposure to diagnostic ultrasound.
- Published in:
- 1990
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- 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
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- Publication type:
- Article
Risk of Fetal Loss in Pregnancies Undergoing Midtrimester Amniocentesis after Inconclusive Chorionic Villus Sampling.
- Published in:
- 2019
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- Publication type:
- journal article
Presence of fetal DNA in maternal plasma decades after pregnancy: further comments.
- Published in:
- Human Genetics, 2002, v. 111, n. 6, p. 576, doi. 10.1007/s00439-002-0797-0
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- Publication type:
- Article
Presence of fetal DNA in maternal plasma decades after pregnancy.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 587, doi. 10.1007/s00439-002-0725-3
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- Publication type:
- Article
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.
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- European Journal of Human Genetics, 2006, v. 14, n. 3, p. 282, doi. 10.1038/sj.ejhg.5201564
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- Publication type:
- Article
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.
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- European Journal of Human Genetics, 2004, v. 12, n. 4, p. 272, doi. 10.1038/sj.ejhg.5201121
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- Publication type:
- Article
Internalization of nanopolymeric tracers does not alter characteristics of placental cells.
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- Journal of Cellular & Molecular Medicine, 2016, v. 20, n. 6, p. 1036, doi. 10.1111/jcmm.12820
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- Publication type:
- Article
Detection of human immunodeficiency virus-1 RNA and DNA by extractive and in situ PCR in unprocessed semen and seminal fractions isolated by semen-washing procedure.
- Published in:
- Human Reproduction, 2006, v. 21, n. 6, p. 1525, doi. 10.1093/humrep/del004
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- Publication type:
- Article
Does confined placental mosaicism affect the fetus?
- Published in:
- 1992
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- Publication type:
- Editorial
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:
- Obituary
Obituary: Bruno Brambati, MD (29 February 1940-3 August 2020).
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.
- Published in:
- 2017
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- Publication type:
- journal article
Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications.
- Published in:
- 2016
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- Publication type:
- journal article
Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.
- Published in:
- 2015
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- 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
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- Publication type:
- journal 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
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- 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
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- 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.
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- Prenatal Diagnosis, 2014, v. 34, n. 5, p. 460, doi. 10.1002/pd.4330
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- Publication type:
- Article
Response to 'QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44 727 first-trimester prenatal diagnoses'.
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- Prenatal Diagnosis, 2013, v. 33, n. 11, p. 1117, doi. 10.1002/pd.4220
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- Publication type:
- Article
QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses.
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- Prenatal Diagnosis, 2013, v. 33, n. 5, p. 502, doi. 10.1002/pd.4099
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- Publication type:
- Article
Application of a new molecular technique for the genetic evaluation of products of conception.
- Published in:
- Prenatal Diagnosis, 2013, v. 33, n. 1, p. 32, doi. 10.1002/pd.4004
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- Publication type:
- Article
Prenatal BACs-on-Beads<sup>TM</sup>: the prospective experience of five prenatal diagnosis laboratories.
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- Prenatal Diagnosis, 2012, v. 32, n. 4, p. 329, doi. 10.1002/pd.2934
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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.
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- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 280, doi. 10.1002/pd.2439
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- Publication type:
- Article
Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.
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- Prenatal Diagnosis, 2004, v. 24, n. 12, p. 997, doi. 10.1002/pd.961
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- Publication type:
- Article