"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 |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 0 | 1 | 1 |
| 1999 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
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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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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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Fassihi H, Eady RA, Mellerio JE, Ashton GH, Dopping-Hepenstal PJ, Denyer JE, Nicolaides KH, Rodeck CH, McGrath JA. Prenatal diagnosis for severe inherited skin disorders: 25 years' experience. Br J Dermatol. 2006 Jan; 154(1):106-13.
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Motaghedi R, Betensky BP, Slowinska B, Cerame B, Cabrer M, New MI, Wilson RC. Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency. J Pediatr Endocrinol Metab. 2005 Feb; 18(2):133-42.
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Cerame BI, Newfield RS, Pascoe L, Curnow KM, Nimkarn S, Roe TF, New MI, Wilson RC. Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia. J Clin Endocrinol Metab. 1999 Sep; 84(9):3129-34.
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Christiano AM, Pulkkinen L, McGrath JA, Uitto J. Mutation-based prenatal diagnosis of Herlitz junctional epidermolysis bullosa. Prenat Diagn. 1997 Apr; 17(4):343-54.
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McGrath JA, Dunnill MG, Christiano AM, Lake BD, Atherton DJ, Rodeck CH, Pope FM, Eady RA, Uitto J. First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus sampling. Br J Dermatol. 1996 Apr; 134(4):734-9.
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McGrath JA, Kivirikko S, Ciatti S, Moss C, Dunnill GS, Eady RA, Rodeck CH, Christiano AM, Uitto J. A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk. Genomics. 1995 Sep 01; 29(1):282-4.
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D'Alton ME, DeCherney AH. Prenatal diagnosis. N Engl J Med. 1993 Jan 14; 328(2):114-20.