142 related articles for article (PubMed ID: 35456449)
21. Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Sahoo T; Dzidic N; Strecker MN; Commander S; Travis MK; Doherty C; Tyson RW; Mendoza AE; Stephenson M; Dise CA; Benito CW; Ziadie MS; Hovanes K
Genet Med; 2017 Jan; 19(1):83-89. PubMed ID: 27337029
[TBL] [Abstract][Full Text] [Related]
22. Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination.
Goumy C; Ouedraogo ZG; Bellemonte E; Eymard-Pierre E; Soler G; Perthus I; Pebrel-Richard C; Gouas L; Salaun G; Véronèse L; Laurichesse H; Darcha C; Tchirkov A
Diagnostics (Basel); 2023 Nov; 13(23):. PubMed ID: 38066817
[TBL] [Abstract][Full Text] [Related]
23. A fast modified protocol for random-access ultra-high density whole-genome scan: a tool for personalized genomic medicine, positional mapping, and cytogenetic analysis.
Lau KC; Mak CM; Leung KY; Tsoi TH; Tang HY; Lee P; Lam CW
Clin Chim Acta; 2009 Aug; 406(1-2):31-5. PubMed ID: 19445911
[TBL] [Abstract][Full Text] [Related]
24. Single-nucleotide polymorphism microarray detects molar pregnancies in 3% of miscarriages.
Maisenbacher MK; Merrion K; Kutteh WH
Fertil Steril; 2019 Oct; 112(4):700-706. PubMed ID: 31395308
[TBL] [Abstract][Full Text] [Related]
25. A tool for mapping Single Nucleotide Polymorphisms using Graphics Processing Units.
Manconi A; Orro A; Manca E; Armano G; Milanesi L
BMC Bioinformatics; 2014; 15 Suppl 1(Suppl 1):S10. PubMed ID: 24564714
[TBL] [Abstract][Full Text] [Related]
26. Systematic evaluation of RNA quality, microarray data reliability and pathway analysis in fresh, fresh frozen and formalin-fixed paraffin-embedded tissue samples.
Wimmer I; Tröscher AR; Brunner F; Rubino SJ; Bien CG; Weiner HL; Lassmann H; Bauer J
Sci Rep; 2018 Apr; 8(1):6351. PubMed ID: 29679021
[TBL] [Abstract][Full Text] [Related]
27. Maternal cell contamination in cultured chorionic villi: comparison of chromosome Q-polymorphisms derived from villi, fetal skin, and maternal lymphocytes.
Williams J; Medearis AL; Chu WH; Kovacs GD; Kaback MM
Prenat Diagn; 1987 Jun; 7(5):315-22. PubMed ID: 3475689
[TBL] [Abstract][Full Text] [Related]
28. Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutional Microarray.
Chaubey A; Shenoy S; Mathur A; Ma Z; Valencia CA; Reddy Nallamilli BR; Szekeres E; Stansberry L; Liu R; Hegde MR
J Mol Diagn; 2020 Jun; 22(6):823-840. PubMed ID: 32344035
[TBL] [Abstract][Full Text] [Related]
29. Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.
Novelli A; Grati FR; Ballarati L; Bernardini L; Bizzoco D; Camurri L; Casalone R; Cardarelli L; Cavalli P; Ciccone R; Clementi M; Dalprà L; Gentile M; Gelli G; Grammatico P; Malacarne M; Nardone AM; Pecile V; Simoni G; Zuffardi O; Giardino D
Ultrasound Obstet Gynecol; 2012 Apr; 39(4):384-8. PubMed ID: 22262341
[TBL] [Abstract][Full Text] [Related]
30. The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use.
D'ippolito S; Di Simone N; Orteschi D; Pomponi MG; Genuardi M; Sisti LG; Castellani R; Rossi ED; Scambia G; Zollino M
PLoS One; 2017; 12(6):e0178113. PubMed ID: 28604823
[TBL] [Abstract][Full Text] [Related]
31. Comprehensive Screening of Gene Copy Number Aberrations in Formalin-Fixed, Paraffin-Embedded Solid Tumors Using Molecular Inversion Probe-Based Single-Nucleotide Polymorphism Array.
Singh RR; Mehrotra M; Chen H; Almohammedsalim AA; Sahin A; Bosamra A; Patel KP; Routbort MJ; Lu X; Ronald A; Mishra BM; Virani S; Medeiros LJ; Luthra R
J Mol Diagn; 2016 Sep; 18(5):676-687. PubMed ID: 27392636
[TBL] [Abstract][Full Text] [Related]
32. Detection of chromosomal aberrations in renal tumors: a comparative study of conventional cytogenetics and virtual karyotyping with single-nucleotide polymorphism microarrays.
Monzon FA; Alvarez K; Gatalica Z; Bridge JA; Nelson M; Kim HJ; Hagenkord JM
Arch Pathol Lab Med; 2009 Dec; 133(12):1917-22. PubMed ID: 19961245
[TBL] [Abstract][Full Text] [Related]
33. Preparation of chorionic villus samples for metaphase chromosome analysis and chromosomal microarray analysis.
Breman A; Patel A
Curr Protoc Hum Genet; 2012 Oct; Chapter 8():Unit8.3. PubMed ID: 23074072
[TBL] [Abstract][Full Text] [Related]
34. Reliability of 46,XX results on miscarriage specimens: a review of 1,222 first-trimester miscarriage specimens.
Lathi RB; Gustin SL; Keller J; Maisenbacher MK; Sigurjonsson S; Tao R; Demko Z
Fertil Steril; 2014 Jan; 101(1):178-82. PubMed ID: 24182409
[TBL] [Abstract][Full Text] [Related]
35. Enhancement of Pathologist's Routine Practice: Reuse of DNA Extracted from Immunostained Formalin-fixed Paraffin-embedded (FFPE) Slides in Downstream Molecular Analysis of Cancer.
Al-Attas A; Assidi M; Al-Maghrabi J; Dallol A; Schulten HJ; Abu-Elmagd M; Chaudhary A; Abuzenadah A; Budowle B; Buhmeida A; Al-Qahtani M
Cancer Genomics Proteomics; 2016 09-10; 13(5):399-406. PubMed ID: 27566658
[TBL] [Abstract][Full Text] [Related]
36. Cost-effectiveness of cytogenetic evaluation of products of conception by chorionic villus sampling in recurrent miscarriage.
Petracchi F; Paez C; Igarzabal L
Prenat Diagn; 2017 Mar; 37(3):282-288. PubMed ID: 28067420
[TBL] [Abstract][Full Text] [Related]
37. Genomic microarray analysis on formalin-fixed paraffin-embedded material for uveal melanoma prognostication.
Minca EC; Tubbs RR; Portier BP; Wang Z; Lanigan C; Aronow ME; Triozzi PL; Singh A; Cook JR; Saunthararajah Y; Plesec TP; Schoenfield L; Cawich V; Sulpizio S; Schultz RA
Cancer Genet; 2014; 207(7-8):306-15. PubMed ID: 25442074
[TBL] [Abstract][Full Text] [Related]
38. Optical Genome Mapping: A Revolutionary Tool for "Next Generation Cytogenomics Analysis" with a Broad Range of Diagnostic Applications in Human Diseases.
Garcia-Heras J
J Assoc Genet Technol; 2021; 47(4):191-200. PubMed ID: 34897113
[TBL] [Abstract][Full Text] [Related]
39. High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays.
Oosting J; Lips EH; van Eijk R; Eilers PH; Szuhai K; Wijmenga C; Morreau H; van Wezel T
Genome Res; 2007 Mar; 17(3):368-76. PubMed ID: 17267813
[TBL] [Abstract][Full Text] [Related]
40. [Application of different technologies for distinguishing true and pseudo mosaicisms during prenatal diagnosis].
Zhu R; Zhu X; Yang Y; Duan H; Zhang Y; Wu X; Wang W; Li J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):636-40. PubMed ID: 25297599
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
