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Items: 1 to 20 of 145

1.

Prenatal genetic testing.

Dolan SM.

Pediatr Ann. 2009 Aug;38(8):426-30. doi: 10.3928/00904481-20090723-05. No abstract available.

PMID:
19711880
2.

From new screens to discovered genes: the successful past and promising present of single gene disorders.

Roe AM, Shur N.

Am J Med Genet C Semin Med Genet. 2007 Feb 15;145C(1):77-86. Review.

PMID:
17315238
3.

Screening for single gene genetic disease.

Musci TJ.

Gynecol Obstet Invest. 2005;60(1):19-26. Epub 2005 Feb 24. Review.

PMID:
15731563
4.

Population-based carrier screening and prenatal diagnosis.

Strom CM.

MLO Med Lab Obs. 2004 Aug;36(8):12-7; quiz 20-1. No abstract available.

PMID:
15366363
5.

Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.

Bailey DB Jr, Skinner D, Davis AM, Whitmarsh I, Powell C.

Pediatrics. 2008 Mar;121(3):e693-704. doi: 10.1542/peds.2007-0820. Review.

PMID:
18310190
6.

Population screening for reproductive risk for single gene disorders in Australia: now and the future.

Delatycki MB.

Twin Res Hum Genet. 2008 Aug;11(4):422-30. doi: 10.1375/twin.11.4.422.

PMID:
18637742
7.

Pediatric cystic fibrosis: evaluating costs and genetic testing.

Balinsky W, Zhu CW.

J Pediatr Health Care. 2004 Jan-Feb;18(1):30-4. Review.

PMID:
14722503
8.

Genetic screening and counseling.

Norton ME.

Curr Opin Obstet Gynecol. 2008 Apr;20(2):157-63. doi: 10.1097/GCO.0b013e3282f73230. Review.

PMID:
18388816
9.

Carrier screening for cystic fibrosis in US genetic testing laboratories: a survey of laboratory directors.

Kaufman DJ, Katsanis SH, Javitt GH, Murphy JA, Scott JA, Hudson KL.

Clin Genet. 2008 Oct;74(4):367-73. doi: 10.1111/j.1399-0004.2008.01070.x. Epub 2008 Aug 12.

PMID:
18700896
10.

Prenatal diagnosis of inherited biochemical disorders. Current and future considerations.

Legge M.

Chin Med J (Engl). 1984 Sep;97(9):671-8. No abstract available.

PMID:
6443300
11.

Cystic fibrosis and fragile X syndrome: the arguments for antenatal screening.

Murray J, Cuckle H.

Comb Chem High Throughput Screen. 2001 May;4(3):265-72. Review.

PMID:
11375741
12.

Genetic screening in reproductive health care.

Mennuti MT.

Clin Obstet Gynecol. 2008 Mar;51(1):3-23. doi: 10.1097/GRF.0b013e318160f241. Review.

PMID:
18303496
13.

Genetic evaluation of oocyte donors: recipient couple preferences and outcome of testing.

Baker VL, Rone HM, Adamson GD.

Fertil Steril. 2008 Dec;90(6):2091-8. doi: 10.1016/j.fertnstert.2007.10.069. Epub 2008 Feb 4.

PMID:
18249390
14.

What is the value for money of prenatal carrier screening for spinal muscular atrophy? Too soon to say.

Grosse SD.

Am J Obstet Gynecol. 2010 Mar;202(3):209-11. doi: 10.1016/j.ajog.2010.01.031. No abstract available.

PMID:
20207235
15.

Prenatal genetics: the evolution and future directions of screening and diagnosis.

Slack C, Lurix K, Lewis S, Lichten L.

J Perinat Neonatal Nurs. 2006 Jan-Mar;20(1):93-7. Review. No abstract available.

PMID:
16508474
16.

Screening for carriers of genetic disease: points to consider.

Haan EA.

Med J Aust. 1993 Mar 15;158(6):419-21. No abstract available.

PMID:
8479358
17.

Genetic testing and medical decision making.

Reyna VF, Lloyd FJ, Whalen P.

Arch Intern Med. 2001 Nov 12;161(20):2406-8. Review. No abstract available.

PMID:
11700152
18.

Fragile X population carrier screening.

Metcalfe SA, Archibald AD, Couns G.

Genet Med. 2012 Mar;14(3):350; author reply 351. doi: 10.1038/gim.2011.79. No abstract available.

PMID:
22391783
19.

Ask the expert. Genetic testing for fragile X.

Prows CA, Lovell AM.

J Soc Pediatr Nurs. 1998 Oct-Dec;3(4):161-6. No abstract available.

PMID:
9884950
20.

Japanese panel OKs IVF screening.

Lamphier M.

Science. 1995 Mar 17;267(5204):1586. No abstract available.

PMID:
7886440

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