Meaney C - Search Results

1

Workshop report on the extraction of foetal DNA from maternal plasma.

Legler TJ, Liu Z, Mavrou A, Finning K, Hromadnikova I, Galbiati S, Meaney C, Hultén MA, Crea F, Olsson ML, Maddocks DG, Huang D, Fisher SA, Sprenger-Haussels M, Soussan AA, van der Schoot CE. Legler TJ, et al. Among authors: meaney c. Prenat Diagn. 2007 Sep;27(9):824-9. doi: 10.1002/pd.1783. Prenat Diagn. 2007. PMID: 17604339

2

Noninvasive prenatal diagnosis of early onset primary dystonia I in maternal plasma.

Meaney C, Norbury G. Meaney C, et al. Prenat Diagn. 2009 Dec;29(13):1218-21. doi: 10.1002/pd.2385. Prenat Diagn. 2009. PMID: 19844939

3

Non-invasive prenatal determination of fetal sex: translating research into clinical practice.

Hill M, Finning K, Martin P, Hogg J, Meaney C, Norbury G, Daniels G, Chitty LS. Hill M, et al. Among authors: meaney c. Clin Genet. 2011 Jul;80(1):68-75. doi: 10.1111/j.1399-0004.2010.01533.x. Epub 2010 Sep 15. Clin Genet. 2011. PMID: 20840219

4

Non-invasive prenatal diagnosis.

Meaney C, Norbury G. Meaney C, et al. Methods Mol Biol. 2011;688:155-72. doi: 10.1007/978-1-60761-947-5_11. Methods Mol Biol. 2011. PMID: 20938838

5

Polymorphous lymphoproliferative disorder with Hodgkin-like features in common γ-chain-deficient severe combined immunodeficiency.

Slatter MA, Angus B, Windebank K, Taylor A, Meaney C, Lester T, Norbury G, Hambleton S, Abinun M, Flood TJ, Cant AJ, Gennery AR. Slatter MA, et al. Among authors: meaney c. J Allergy Clin Immunol. 2011 Feb;127(2):533-5. doi: 10.1016/j.jaci.2010.09.036. Epub 2010 Nov 20. J Allergy Clin Immunol. 2011. PMID: 21094519 No abstract available.

6

New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma.

Chitty LS, Griffin DR, Meaney C, Barrett A, Khalil A, Pajkrt E, Cole TJ. Chitty LS, et al. Among authors: meaney c. Ultrasound Obstet Gynecol. 2011 Mar;37(3):283-9. doi: 10.1002/uog.8893. Epub 2011 Feb 1. Ultrasound Obstet Gynecol. 2011. PMID: 21105021 Free article.

7

Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutations.

Beesley CE, Meaney CA, Greenland G, Adams V, Vellodi A, Young EP, Winchester BG. Beesley CE, et al. Among authors: meaney ca. Hum Genet. 2001 Nov;109(5):503-11. doi: 10.1007/s004390100606. Epub 2001 Oct 19. Hum Genet. 2001. PMID: 11735025

8

A common 2 bp deletion mutation in the glucose-6-phosphatase gene in Indian patients with glycogen storage disease type Ia.

Meaney C, Cranston T, Lee P, Genet S. Meaney C, et al. J Inherit Metab Dis. 2001 Aug;24(4):517-8. doi: 10.1023/a:1010598109582. J Inherit Metab Dis. 2001. PMID: 11596659

9

Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency.

Eastwood D, Gilmour KC, Nistala K, Meaney C, Chapel H, Sherrell Z, Webster AD, Davies EG, Jones A, Gaspar HB. Eastwood D, et al. Among authors: meaney c. Clin Exp Immunol. 2004 Sep;137(3):584-8. doi: 10.1111/j.1365-2249.2004.02581.x. Clin Exp Immunol. 2004. PMID: 15320910 Free PMC article.

10

The postnatal features of bent bone dysplasia-FGFR2 type.

Scott RH, Meaney C, Jenkins L, Calder A, Hurst JA. Scott RH, et al. Among authors: meaney c. Clin Dysmorphol. 2014 Jan;23(1):8-11. doi: 10.1097/MCD.0000000000000022. Clin Dysmorphol. 2014. PMID: 24300289 No abstract available.

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