Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening-Reference-Cited by-同舟云学术

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Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening

Published:1989-03 Issue:4 Volume:81 Page:363-366
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Jinks David C.,Minter Mikeanne,Tarver Deborah A.,Vanderford Mindy,Hejtmancik J. Fielding,McCabe Edward R. B.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00283692.pdf

Reference27 articles.

1. Caskey CT (1987) Disease diagnosis by recombinant DNA methods. Science 236:1223–1229

2. Conner BJ, Reyes AA, Morin C, Itakura K, Teplitz RL, Wallace RB (1983) Detection of sickle cell βS-globin allele by hybridization with synthetic oligonucleotides. Proc Natl Acad Sci USA 80:278–282

3. Covone AE, Mutton D, Johnson PM, Adinolfi M (1984) Trophoblast cells in the peripheral blood from pregnant women. Lancet II: 841–843

4. DiLella AG, Huang W-M, Woo SLC (1988) Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction. Lancet I:497–499

5. Embury SH, Scharf SJ, Saiki RK, Gholson MA, Golbus M, Arnheim N, Erlich HA (1987) Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis. N Engl J Med 316: 656–661

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