Literature DB >> 2393030

Defining DNA diagnostic tests appropriate or standard clinical care.

R V Lebo1, G Cunningham, M J Simons, L J Shapiro.   

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Year:  1990        PMID: 2393030      PMCID: PMC1683880     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  53 in total

1.  Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene.

Authors:  G R Cutting; S E Antonarakis; K H Buetow; L M Kasch; B J Rosenstein; H H Kazazian
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

2.  Identification and characterization of nine RFLPs at the adenosine deaminase (ADA) locus.

Authors:  S Tzall; A Ellenbogen; F Eng; R Hirschhorn
Journal:  Am J Hum Genet       Date:  1989-06       Impact factor: 11.025

3.  Molecular screening for haemoglobin constant spring.

Authors:  Y E Hsia; C A Ford; L J Shapiro; J A Hunt; N S Ching
Journal:  Lancet       Date:  1989-05-06       Impact factor: 79.321

4.  Regional localization of the autosomal dominant polycystic kidney disease locus.

Authors:  S T Reeders; T Keith; P Green; G G Germino; N J Barton; O J Lehmann; V A Brown; P Phipps; J Morgan; J C Bear
Journal:  Genomics       Date:  1988-08       Impact factor: 5.736

5.  Linkage disequilibrium, cystic fibrosis, and genetic counseling.

Authors:  A L Beaudet; G L Feldman; S D Fernbach; G J Buffone; W E O'Brien
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

6.  Rapid prenatal diagnosis of beta thalassemia using DNA amplification and nonradioactive probes.

Authors:  S P Cai; C A Chang; J Z Zhang; R K Saiki; H A Erlich; Y W Kan
Journal:  Blood       Date:  1989-02       Impact factor: 22.113

7.  Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome.

Authors:  N Dahl; K Hammarström-Heeroma; P Goonewardena; C Wadelius; K H Gustavson; G Holmgren; G J van Ommen; U Pettersson
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

8.  Mapping of recombinants near the Huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4S10 region.

Authors:  M I Skraastad; E Bakker; L F de Lange; M Vegter-van der Vlis; E G Klein-Breteler; G J van Ommen; P L Pearson
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

9.  A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.

Authors:  G Singh; M T Lott; D C Wallace
Journal:  N Engl J Med       Date:  1989-05-18       Impact factor: 91.245

10.  Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

Authors:  C T Moraes; S DiMauro; M Zeviani; A Lombes; S Shanske; A F Miranda; H Nakase; E Bonilla; L C Werneck; S Servidei
Journal:  N Engl J Med       Date:  1989-05-18       Impact factor: 91.245

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  1 in total

1.  Immune Responses in Malaria and Vaccine Strategies.

Authors:  Janez Ferluga; Iesha Singh; Sashmita Rout; Ahmed Al-Qahtani; Hadida Yasmin; Uday Kishore
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

  1 in total

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