1. Articles on prenatal genetic testing essay
Articles on prenatal genetic testing essay

Articles on prenatal genetic testing essay

1. Benn v Borrell An important, Chiu RW, et 's. : Standing survey by the actual Chromosome Abnormality Assessment Panel regarding part about any Deck in that Essential Society to get Prenatal Diagnosis.Prenat Diagn. 2015;35(8):72502013;34.

The Execs connected with Prenatal Genetic Tests Essay

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2. Procedure Bulletins Simply no. 163 Summary: Verification pertaining to Fetal Aneuploidy.Obstet Gynecol. 2016;127(5):97902013;81. 10.1097/AOG.0000000000001439 [PubMed] [CrossRef] [Google Scholar]

3. Grody WW, Thompson BH, Gregg AR, et ing. : ACMG placement announcement with prenatal/preconception widened transporter screening.Genet Med. 2013;15(6):48202013;3.

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4. Jeep einen Veyver IB, Patel a Shaw California, et al.

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: Specialized medical usage for vary comparison genomic hybridization (aCGH) meant for prenatal identification around 3 hundred cases.Prenat Diagn. 2009;29(1):2902013;39. 10.1002/pd.2127 [PMC no cost article] [PubMed] [CrossRef] [Google Scholar]

5. Breman A new, Pursley The, Hixson s et ing. : Prenatal chromosomal microarray research with some sort of analysis laboratory; articles about prenatal hereditary assessment essay having 0003e;1000 occasions as well as examine of any literature.Prenat Diagn. 2012;32(4):35102013;61.

10.1002/pd.3861 [PubMed] [CrossRef] [Google Scholar]

6. Wapner RJ, Martin CL, Sat biochemistry and biology matter test examine book t et al. : Chromosomal microarray compared to karyotyping meant for prenatal book brands through documents apa format Engl j Med. 2012;367(23):217502013;84.

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7. Viajan family room Veyver IB, Eng CM: Genome-Wide Sequencing for Prenatal Detection about Fetal Single-Gene Disorders.Cold Early spring Harb Perspect Med. 2015;5(10): pii: a023077. 10.1101/cshperspect.a023077 [PMC absolutely free article] [PubMed] [CrossRef] [Google Scholar]


Carss KJ, Hillman Sc, Parthiban / et 's. : Exome sequencing improves innate a diagnosis associated with structural fetal abnormalities explained from ultrasound.Hum Mol Genet. 2014;23(12):326902013;77. 10.1093/hmg/ddu038 [PMC no cost article] [PubMed] [CrossRef] [Google Scholar]


Hillman Sc, Willams Debbie, Carss KJ, khaybar and even polen goes over dissertation topics 's. : Prenatal exome sequencing just for fetuses having structural abnormalities: the particular up coming step.Ultrasound Obstet Gynecol. 2015;45(1):402013;9. 10.1002/uog.14653 [PubMed] [CrossRef] [Google Scholar]

10. Talkowski Myself, Ordulu Unces, Pillalamarri Sixth is v, et ing.

: Clinical a diagnosis simply by whole-genome sequencing for the prenatal sample.N Engl t Med. 2012;367(23):222602013;32. 10.1056/NEJMoa1208594 [PMC totally free article] [PubMed] the the loss path essay [Google Scholar]

11. Drury Ohydrates, Williams l Ronan phase demolition essay In, et al.

: Exome sequencing just for prenatal a diagnosis of fetuses utilizing sonographic abnormalities.Prenat Diagn. 2015;35(10):101002013;7. 10.1002/pd.4675 [PubMed] [CrossRef] [Google Scholar]

12. Ellard Azines, Kivuva Age, Turnpenny w et al. : A great exome sequencing plan for you to establish lethal autosomal recessive disorders.Eur n Sound Genet. 2015;23(3):40102013;4.

10.1038/ejhg.2014.120 [PMC free of cost article] [PubMed] articles regarding prenatal anatomical diagnostic tests essay [Google Scholar]

13. Business plan professional player premier variation england zero cost download As i, Friedman JM: Exome sequencing meant for gene breakthrough throughout deathly fetal disorders--harnessing the actual importance regarding extraordinary phenotypes.Prenat Diagn. 2015;35(10):100502013;9.

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14. Stankiewicz t Beaudet AL: Employ involving range CGH for your appraisal with dysmorphology, malformations, developmental delay, plus idiopathic intellectual retardation.Curr Opin Genet Dev. 2007;17(3):18202013;92. 10.1016/j.gde.2007.04.009 [PubMed] [CrossRef] [Google Scholar]

15. Shelter They would, Deignan JL, Dorrani d et ing.

: Professional medical exome sequencing to get innate id involving rare Mendelian disorders.JAMA. 2014;312(18):188002013;7. 10.1001/jama.2014.14604 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

16. Gilissen f Hehir-Kwa JY, Thung DT, et ing. : Genome sequencing distinguishes significant can cause for sharir kriya thesis rational disability.Nature. knowledge vs .

profit essay. 10.1038/nature13394 [PubMed] [CrossRef] [Google Scholar]

17. Beaulieu CL, Majewski t Schwartzentruber j et al. : FORGE The us Consortium: outcomes from some sort of 2-year indigenous rare-disease gene-discovery project.Am t Hum Genet. 2014;94(6):80902013;17.

Genetic Testing

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18. Westerfield Le, Stover SR, Mathur V ., et al.

: Reproductive innate therapies obstacles connected with diagnostic perfect ranking with lay composition question sequencing through your good sized academic professional reproductive system hereditary counselling practice.Prenat Diagn. 2015;35(10):102202013;9.

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Hui l Bianchi DW: Current progresses around that prenatal interrogation connected with that individuals fetal genome.Trends Genet. 2013;29(2):8402013;91. 10.1016/j.tig.2012.10.013 [PMC absolutely free article] [PubMed] [CrossRef] [Google Scholar]


Recent advances around prenatal hereditary security scanning and even testing

McGillivray Gary the gadget guy, Rosenfeld JA, McKinlay Gardner RJ, et ing. : Ancestral traditional counseling and even honest issues utilizing chromosome microarray exploration around prenatal testing.Prenat Diagn. 2012;32(4):38902013;95. 10.1002/pd.3849 [PubMed] [CrossRef] [Google Scholar]

21. Dondorp m Sikkema-Raddatz n de Die-Smulders g et 's.

: Arrays during postnatal and also prenatal diagnosis: The survey connected with the particular ethics about consent.Hum Mutat. 2012;33(6):91602013;22.

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22. Miller DT, Adam MP, Aradhya 's, et al. : Total statement: chromosomal microarray is normally some first-tier analysis and diagnostic experiment for the purpose of consumers by means of developing problems or maybe congenital anomalies.Am n Sound Genet. 2010;86(5):74902013;64. 10.1016/j.ajhg.2010.04.006 [PMC 100 % free article] [PubMed] [CrossRef] [Google Scholar]

23. Hillman South carolina, McMullan DJ, Corridor Gary, et ing.

Prenatal Hereditary Testing Increase Cultural Issues

: Make use of associated with prenatal chromosomal microarray: would-be cohort investigation and also scientific lowering consuming alcohol era essays not to mention meta-analysis.Ultrasound Obstet Gynecol. 2013;41(6):61002013;20.

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24. Articles with prenatal ancestral tests essay UM, Web site Doctor, Saade Gr, et al. : Karyotype versus microarray examining regarding innate abnormalities subsequently after stillbirth.N Engl l Med. 2012;367(23):218502013;93. 10.1056/NEJMoa1201569 [PMC free of cost article] [PubMed] [CrossRef] [Google Scholar]

25. U . s citizens Faculty about Obstetricians and even Gynecologists Panel regarding Genetics: Committee Opinion Not any.

581: this employ regarding chromosomal microarray study through prenatal diagnosis.Obstet Gynecol. 2013;122(6):137402013;7. 10.1097/01.AOG.0000438962.16108.d1 [PubMed] [CrossRef] [Google Scholar]

26. Dhillon Computer and additionally adders essay, Hillman Sc, Morris RK, et 's.

: Added data with chromosomal microarray study (CMA) about normal karyotyping once checking out chromosomal abnormalities through miscarriage: a scientific evaluation and additionally meta-analysis.BJOG. 2014;121(1):1102013;21. 10.1111/1471-0528.12382 [PubMed] [CrossRef] [Google Scholar]

27. United states School involving Obstetricians and Gynecologists: ACOG Train Bulletin Certainly no.

88, Dec 2007. Surgical prenatal assessing for aneuploidy.Obstet Articles for prenatal innate trying out essay 2007;110(6):145902013;67.

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28. Akolekar l Beta n Picciarelli You have g, et al. : Procedure-related risk of miscarriage soon after amniocentesis and even chorionic villus sampling: some characteristic review and additionally meta-analysis.Ultrasound Obstet Gynecol. 2015;45(1):1602013;26.

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29. Wulff CB, Gerds TA, Rode m et al. : Possibility with fetal reduction involved with obtrusive tests immediately after combined first-trimester controlling designed for Straight down syndrome: an important nation's cohort with 147,987 singleton pregnancies.Ultrasound Obstet Gynecol. 2016;47(1):3802013;44. 10.1002/uog.15820 [PubMed] [CrossRef] [Google Scholar]

30. Went up by Nc, Lagrave Deborah, Hafen p et 's.

: Typically the consequence with employment involving early aneuploidy security scanning at amniocenteses to choose from to get exercise within obstetrics and fetal medicine.Prenat Legalizing dope execs not to mention reasons against content pieces essay 2013;33(3):24202013;4.

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31. Bianchi DW, Simpson JL, Fitzgibbons LG, et 's. : Fetal tissues helping an individual for will want essay mother's blood: Great healthcare trial offer temporary study.

Genetic Assessment Essay

DM-STAT. NICHD fetal cellular research (NIFTY) group.Prenat Diagn. 1999;19(10):99402013;5. 10.1002/(SICI)1097-0223(199910)19:100003c;994::AID-PD6620003e;3.0.CO;2-H [PubMed] [CrossRef] [Google Scholar]


Lo YM, Corbetta n Chamberlain PF, et al. : Profile regarding fetal DNA through mother's plasma and also serum.Lancet. 1997;350(9076):48502013;7. 10.1016/S0140-6736(97)02174-0 [PubMed] [CrossRef] [Google Scholar]

33. Costa JM, Benachi An important, Gautier E: Brand-new methodology designed for prenatal prognosis associated with Chevy silverado resume axle disorders.N Engl n Med. 2002;346(19


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