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217 results

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Page 1
First trimester diagnosis and screening for fetal aneuploidy.
Driscoll DA, Gross SJ; Professional Practice and Guidelines Committee. Driscoll DA, et al. Among authors: gross sj. Genet Med. 2008 Jan;10(1):73-5. doi: 10.1097/GIM.0b013e31815efde8. Genet Med. 2008. PMID: 18197059 Free PMC article.
Clinical practice. Prenatal screening for aneuploidy.
Driscoll DA, Gross S. Driscoll DA, et al. N Engl J Med. 2009 Jun 11;360(24):2556-62. doi: 10.1056/NEJMcp0900134. N Engl J Med. 2009. PMID: 19516035 Review. No abstract available.
Screening for fetal aneuploidy and neural tube defects.
Driscoll DA, Gross SJ; Professional Practice Guidelines Committee. Driscoll DA, et al. Among authors: gross sj. Genet Med. 2009 Nov;11(11):818-21. doi: 10.1097/GIM.0b013e3181bb267b. Genet Med. 2009. PMID: 19915395 Free PMC article.
Indications for genetic referral: a guide for healthcare providers.
Pletcher BA, Toriello HV, Noblin SJ, Seaver LH, Driscoll DA, Bennett RL, Gross SJ. Pletcher BA, et al. Among authors: gross sj. Genet Med. 2007 Jun;9(6):385-9. doi: 10.1097/gim.0b013e318064e70c. Genet Med. 2007. PMID: 17575505 Free PMC article.
The future is now: carrier screening for all populations.
Pletcher BA, Gross SJ, Monaghan KG, Driscoll DA, Watson MS. Pletcher BA, et al. Among authors: gross sj. Genet Med. 2008 Jan;10(1):33-6. doi: 10.1097/GIM.0b013e31815f5934. Genet Med. 2008. PMID: 18197054 Free article. Review. No abstract available.
Carrier screening in individuals of Ashkenazi Jewish descent.
Gross SJ, Pletcher BA, Monaghan KG; Professional Practice and Guidelines Committee. Gross SJ, et al. Genet Med. 2008 Jan;10(1):54-6. doi: 10.1097/GIM.0b013e31815f247c. Genet Med. 2008. PMID: 18197057 Free PMC article.
ACMG statement on noninvasive prenatal screening for fetal aneuploidy.
Gregg AR, Gross SJ, Best RG, Monaghan KG, Bajaj K, Skotko BG, Thompson BH, Watson MS. Gregg AR, et al. Among authors: gross sj. Genet Med. 2013 May;15(5):395-8. doi: 10.1038/gim.2013.29. Epub 2013 Apr 4. Genet Med. 2013. PMID: 23558255 Free article.
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.
Gross SJ, Stosic M, McDonald-McGinn DM, Bassett AS, Norvez A, Dhamankar R, Kobara K, Kirkizlar E, Zimmermann B, Wayham N, Babiarz JE, Ryan A, Jinnett KN, Demko Z, Benn P. Gross SJ, et al. Ultrasound Obstet Gynecol. 2016 Feb;47(2):177-83. doi: 10.1002/uog.15754. Epub 2016 Jan 5. Ultrasound Obstet Gynecol. 2016. PMID: 26396068 Free PMC article.
First-trimester or second-trimester screening, or both, for Down's syndrome.
Malone FD, Canick JA, Ball RH, Nyberg DA, Comstock CH, Bukowski R, Berkowitz RL, Gross SJ, Dugoff L, Craigo SD, Timor-Tritsch IE, Carr SR, Wolfe HM, Dukes K, Bianchi DW, Rudnicka AR, Hackshaw AK, Lambert-Messerlian G, Wald NJ, D'Alton ME; First- and Second-Trimester Evaluation of Risk (FASTER) Research Consortium. Malone FD, et al. Among authors: gross sj. N Engl J Med. 2005 Nov 10;353(19):2001-11. doi: 10.1056/NEJMoa043693. N Engl J Med. 2005. PMID: 16282175 Free article. Clinical Trial.
Prenatal screening and diagnosis--An introduction.
Gross S, Cuckle H. Gross S, et al. Am J Med Genet C Semin Med Genet. 2007 Feb 15;145C(1):1-4. doi: 10.1002/ajmg.c.30122. Am J Med Genet C Semin Med Genet. 2007. PMID: 17304543 No abstract available.
217 results