Kellner LH - Search Results

1

Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population.

Rady PL, Tyring SK, Hudnall SD, Vargas T, Kellner LH, Nitowsky H, Matalon RK. Rady PL, et al. Among authors: kellner lh. Am J Med Genet. 1999 Oct 8;86(4):380-4. doi: 10.1002/(sici)1096-8628(19991008)86:4<380::aid-ajmg13>3.0.co;2-9. Am J Med Genet. 1999. PMID: 10494095

2

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

Rady PL, Szucs S, Grady J, Hudnall SD, Kellner LH, Nitowsky H, Tyring SK, Matalon RK. Rady PL, et al. Among authors: kellner lh. Am J Med Genet. 2002 Jan 15;107(2):162-8. doi: 10.1002/ajmg.10122. Am J Med Genet. 2002. PMID: 11807892

3

Comprehensive analysis of genetic polymorphisms in the interleukin-10 promoter: implications for immune regulation in specific ethnic populations.

Rady PL, Matalon R, Grady J, Smith EM, Hudnall SD, Kellner LH, Nitowsky H, Tyring SK, Hughes TK. Rady PL, et al. Among authors: kellner lh. Genet Test. 2004 Summer;8(2):194-203. doi: 10.1089/gte.2004.8.194. Genet Test. 2004. PMID: 15345120

4

Genetic polymorphism (G80A) of reduced folate carrier gene in ethnic populations.

Rady PL, Szucs S, Matalon RK, Grady J, Hudnall SD, Kellner LH, Nitowsky H. Rady PL, et al. Among authors: kellner lh. Mol Genet Metab. 2001 Jul;73(3):285-6. doi: 10.1006/mgme.2001.3197. Mol Genet Metab. 2001. PMID: 11461197 No abstract available.

5

Incorporation of fetal DNA detection assay in a noninvasive RhD diagnostic test.

Li Y, Kazzaz JA, Kellner LH, Brown SA. Li Y, et al. Among authors: kellner lh. Prenat Diagn. 2010 Oct;30(10):1010-2. doi: 10.1002/pd.2598. Prenat Diagn. 2010. PMID: 20721880 No abstract available.

6

Quality assessment of routine nuchal translucency measurements: a North American laboratory perspective.

Palomaki GE, Neveux LM, Donnenfeld A, Lee JE, McDowell G, Canick JA, Summers A, Lambert-Messerlian G, Kellner LH, Zebelman A, Haddow JE. Palomaki GE, et al. Among authors: kellner lh. Genet Med. 2008 Feb;10(2):131-8. doi: 10.1097/GIM.0b013e3181616bf8. Genet Med. 2008. PMID: 18281921 Free article.

7

Anomalous marker patterns in Down syndrome screening.

Wald NJ, Bestwick JP, Barnes IM, Kellner LH. Wald NJ, et al. Among authors: kellner lh. Prenat Diagn. 2007 Feb;27(2):185-6. doi: 10.1002/pd.1633. Prenat Diagn. 2007. PMID: 17266168 No abstract available.

8

Maternal serum alpha-fetoprotein and human chorionic gonadotropin levels in women with human immunodeficiency virus.

Kellner LH, Mizejewski GI. Kellner LH, et al. Am J Obstet Gynecol. 2004 Jul;191(1):384-5. doi: 10.1016/j.ajog.2003.11.014. Am J Obstet Gynecol. 2004. PMID: 15309762 No abstract available.

9

Prenatal screening for open neural tube defects.

Canick JA, Kellner LH, Bombard AT. Canick JA, et al. Among authors: kellner lh. Clin Lab Med. 2003 Jun;23(2):385-94, ix. doi: 10.1016/s0272-2712(03)00032-5. Clin Lab Med. 2003. PMID: 12848450 Review.

10

Maternal serum levels of type I and type III procollagen peptides in pre-eclamptic pregnancy.

Yamamoto H, Lambert-Messerlian GM, Silver HM, Kudo R, Kellner LH, Canick JA. Yamamoto H, et al. Among authors: kellner lh. J Matern Fetal Med. 2001 Feb;10(1):40-3. doi: 10.1080/714904294. J Matern Fetal Med. 2001. PMID: 11332418

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