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Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.
Martin, K; Iyengar, S; Kalyan, A; Lan, C; Simon, A L; Stosic, M; Kobara, K; Ravi, H; Truong, T; Ryan, A; Demko, Z P; Benn, P.
Affiliation
  • Martin K; Natera, Inc., San Carlos, California.
  • Iyengar S; Natera, Inc., San Carlos, California.
  • Kalyan A; Natera, Inc., San Carlos, California.
  • Lan C; Natera, Inc., San Carlos, California.
  • Simon AL; Natera, Inc., San Carlos, California.
  • Stosic M; Natera, Inc., San Carlos, California.
  • Kobara K; Natera, Inc., San Carlos, California.
  • Ravi H; Natera, Inc., San Carlos, California.
  • Truong T; Natera, Inc., San Carlos, California.
  • Ryan A; Natera, Inc., San Carlos, California.
  • Demko ZP; Natera, Inc., San Carlos, California.
  • Benn P; Department of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, Connecticut.
Clin Genet ; 93(2): 293-300, 2018 02.
Article in En | MEDLINE | ID: mdl-28696552
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Angelman Syndrome / Polymorphism, Single Nucleotide / DiGeorge Syndrome Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Pregnancy Language: En Journal: Clin Genet Year: 2018 Type: Article
Fulltext
Print
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Angelman Syndrome / Polymorphism, Single Nucleotide / DiGeorge Syndrome Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Pregnancy Language: En Journal: Clin Genet Year: 2018 Type: Article