"Chorionic Villi Sampling" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A method for diagnosis of fetal diseases by sampling the cells of the placental chorionic villi for DNA analysis, presence of bacteria, concentration of metabolites, etc. The advantage over amniocentesis is that the procedure can be carried out in the first trimester.
| Descriptor ID |
D015193
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| MeSH Number(s) |
E01.370.225.500.384.100.149 E01.370.225.998.054.149 E01.370.378.630.150 E01.370.388.100.150 E04.074.149 E05.200.500.384.100.149 E05.200.998.054.149 E05.242.384.100.149
|
| Concept/Terms |
Chorionic Villi Sampling- Chorionic Villi Sampling
- Chorionic Villi Samplings
- Sampling, Chorionic Villi
- Samplings, Chorionic Villi
- Biopsy, Chorionic Villi
- Biopsies, Chorionic Villi
- Chorionic Villi Biopsies
- Chorionic Villi Biopsy
- Chorionic Villus Sampling
- Chorionic Villus Samplings
- Sampling, Chorionic Villus
- Samplings, Chorionic Villus
|
Below are MeSH descriptors whose meaning is more general than "Chorionic Villi Sampling".
Below are MeSH descriptors whose meaning is more specific than "Chorionic Villi Sampling".
This graph shows the total number of publications written about "Chorionic Villi Sampling" by people in this website by year, and whether "Chorionic Villi Sampling" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2006 | 0 | 2 | 2 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 1 | 1 | 2 |
| 2017 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Chorionic Villi Sampling" by people in Profiles.
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Al-Ibraheemi Z, Rosenn B, Porat N, Taylor D, Kalberer M, Nelson Z. Changing Face of Invasive Diagnostic Testing in the Era of Cell-Free DNA. Am J Perinatol. 2017 09; 34(11):1142-1147.
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Bornstein E, Lenchner E, Donnenfeld A, Jodicke C, Keeler SM, Kapp S, Divon MY. Complete trisomy 21 vs translocation Down syndrome: a comparison of modes of ascertainment. Am J Obstet Gynecol. 2010 Oct; 203(4):391.e1-5.
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Fassihi H, McGrath JA. Prenatal diagnosis of epidermolysis bullosa. Dermatol Clin. 2010 Apr; 28(2):231-7, viii.
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Treff NR, Su J, Tao X, Miller KA, Levy B, Scott RT. A novel single-cell DNA fingerprinting method successfully distinguishes sibling human embryos. Fertil Steril. 2010 Jul; 94(2):477-84.
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Annable K, Donnenfeld AE, Fischer RL, Knops J. Prenatal diagnosis of a jumping translocation. Prenat Diagn. 2008 Aug; 28(8):767-9.
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McClarren J, Donnenfeld AE, Ravnan JB. Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion. Prenat Diagn. 2006 Dec; 26(13):1212-5.
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Donnenfeld AE, Cutillo D, Horwitz J, Knops J. Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency. Am J Obstet Gynecol. 2006 Feb; 194(2):508-11.
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Jenkins TM, Sciscione AC, Wapner RJ, Sarto GE. Training in chorionic villus sampling: limited experience for US fellows. Am J Obstet Gynecol. 2004 Oct; 191(4):1288-90.
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Pfendner EG, Nakano A, Pulkkinen L, Christiano AM, Uitto J. Prenatal diagnosis for epidermolysis bullosa: a study of 144 consecutive pregnancies at risk. Prenat Diagn. 2003 Jun; 23(6):447-56.
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Al-Kouatly HB, Chasen ST, Gilbert F, Ahner R, Alonso LM, Chervenak FA. Correlation between rare chromosomal abnormalities and prenatal ultrasound findings. Am J Med Genet. 2002 Jan 22; 107(3):197-200.