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Results: 1 to 20 of 21

Related Articles by Review for PubMed (Select 20331943)

1.

Complications associated with carrier status among people with blood disorders: a commentary.

Hooper WC, Miller CH, Key NS.

Am J Prev Med. 2010 Apr;38(4 Suppl):S456-8. doi: 10.1016/j.amepre.2010.01.009. No abstract available.

PMID:
20331943
2.

Carrier screening for cystic fibrosis: a perinatal perspective.

Demsey SA.

J Perinat Neonatal Nurs. 1999 Sep;13(2):14-26. Review.

PMID:
10818851
3.

Carrier detection and prenatal screening of the retinoblastoma gene.

Cowell JK, Onadim Z.

J Pathol. 1990 May;161(1):3-5. Review. No abstract available.

PMID:
2196349
4.

Variable clinical phenotypes of alpha-thalassemia syndromes.

Singer ST.

ScientificWorldJournal. 2009 Jul 13;9:615-25. doi: 10.1100/tsw.2009.69. Review.

5.

It's "back to school" for genetic screening.

Gason AA, Delatycki MB, Metcalfe SA, Aitken M.

Eur J Hum Genet. 2006 Apr;14(4):384-9. Review.

6.

Carrier screening and prenatal diagnosis of beta-thalassemia.

Maheshwari M, Arora S, Kabra M, Menon PS.

Indian Pediatr. 1999 Nov;36(11):1119-25. Review. No abstract available.

PMID:
10745333
7.

Carrier testing in minors: a systematic review of guidelines and position papers.

Borry P, Fryns JP, Schotsmans P, Dierickx K.

Eur J Hum Genet. 2006 Feb;14(2):133-8. Review.

8.

Thalassaemia control in developing countries--the Sri Lankan perspective.

Perera DM, Gunasekara D, Wijekoon A, Petrou M.

Ceylon Med J. 2000 Mar;45(1):12-6. Review.

PMID:
11006614
9.

[Carrier state of x-linked adrenoleukodystrophy].

van Geel BM.

Ned Tijdschr Geneeskd. 2000 Sep 9;144(37):1764-8. Review. Dutch.

PMID:
11004948
10.

Carrier detection and prenatal diagnosis of hemophilia in developing countries.

Peyvandi F.

Semin Thromb Hemost. 2005 Nov;31(5):544-54. Review.

PMID:
16276463
11.

Preventive aspects of genetic morbidity: experiences of the Canadian model.

Khalifa MM.

East Mediterr Health J. 1999 Nov;5(6):1121-8. Review.

PMID:
11924099
12.

Genetic red cell disorders in Saudi Arabia: a multifaceted problem.

el-Hazmi MA.

Hemoglobin. 1994 May;18(3):257-68. Review. No abstract available.

PMID:
7928385
13.

Carrier testing for autosomal-recessive disorders.

Vallance H, Ford J.

Crit Rev Clin Lab Sci. 2003 Aug;40(4):473-97. Review.

PMID:
14582604
14.
15.

To know or not to know: a review of behaviour and suicidal ideation in preclinical Huntington's disease.

Robins Wahlin TB.

Patient Educ Couns. 2007 Mar;65(3):279-87. Epub 2006 Sep 26. Review.

PMID:
17000074
16.

Complex phenotypes in the haemoglobinopathies: recommendations on screening and DNA testing.

Trent RJ, Webster B, Bowden DK, Gilbert A, Holl PJ, Lindeman R, Lammi A, Rowell J, Hinchcliffe M, Colley A, Wilson M, Saleh M, Blackwell J, Petrou V.

Pathology. 2006 Dec;38(6):507-19. Review.

PMID:
17393977
17.

Prenatal diagnosis of inherited blood diseases.

Weatherall DJ.

Clin Haematol. 1985 Oct;14(3):747-74. Review.

PMID:
3907916
18.

Recent advances in haematology.

Provan D, O'Shaughnessy DF.

BMJ. 1999 Apr 10;318(7189):991-4. Review. No abstract available.

19.

Screening for thalassemia: a model of success.

Cao A, Rosatelli MC, Monni G, Galanello R.

Obstet Gynecol Clin North Am. 2002 Jun;29(2):305-28, vi-vii. Review.

PMID:
12108831
20.

Heterozygote screening for Tay-Sachs disease: past successes and future challenges.

Natowicz MR, Prence EM.

Curr Opin Pediatr. 1996 Dec;8(6):625-9. Review.

PMID:
9018448
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