Read AP - Search Results

1

Read's Recall: Shuffling abstracts - and foundations.

Read AP. Read AP. Eur J Hum Genet. 2017 Dec;25(s2):S27-S28. doi: 10.1038/ejhg.2017.149. Eur J Hum Genet. 2017. PMID: 29297877 Free PMC article. No abstract available.

2

What can be offered to couples at (possibly) increased genetic risk?

Read AP, Donnai D. Read AP, et al. J Community Genet. 2012 Jul;3(3):167-74. doi: 10.1007/s12687-012-0105-1. Epub 2012 Jul 4. J Community Genet. 2012. PMID: 22760671 Free PMC article.

3

Apparent prevention of neural tube defects by periconceptional vitamin supplementation. 1981.

Smithells RW, Sheppard S, Schorah CJ, Seller MJ, Nevin NC, Harris R, Read AP, Fielding DW. Smithells RW, et al. Among authors: read ap. Int J Epidemiol. 2011 Oct;40(5):1146-54. doi: 10.1093/ije/dyr143. Int J Epidemiol. 2011. PMID: 22039189

4

The genetics of otosclerosis: pedigree studies and linkage analysis.

Saeed SR, Briggs M, Lobo C, Al-Zoubi F, Ramsden RT, Read AP. Saeed SR, et al. Among authors: read ap. Adv Otorhinolaryngol. 2007;65:75-85. doi: 10.1159/000098675. Adv Otorhinolaryngol. 2007. PMID: 17245027

5

Phenotypic variation in constitutional delay of growth and puberty: relationship to specific leptin and leptin receptor gene polymorphisms.

Banerjee I, Trueman JA, Hall CM, Price DA, Patel L, Whatmore AJ, Hirschhorn JN, Read AP, Palmert MR, Clayton PE. Banerjee I, et al. Among authors: read ap. Eur J Endocrinol. 2006 Jul;155(1):121-6. doi: 10.1530/eje.1.02184. Eur J Endocrinol. 2006. PMID: 16793957

6

GTF2IRD1 in craniofacial development of humans and mice.

Tassabehji M, Hammond P, Karmiloff-Smith A, Thompson P, Thorgeirsson SS, Durkin ME, Popescu NC, Hutton T, Metcalfe K, Rucka A, Stewart H, Read AP, Maconochie M, Donnai D. Tassabehji M, et al. Among authors: read ap. Science. 2005 Nov 18;310(5751):1184-7. doi: 10.1126/science.1116142. Epub 2005 Nov 3. Science. 2005. PMID: 16293761

7

Inherited eye disease: cause and late effect.

Manson FD, Trump D, Read AP, Black GC. Manson FD, et al. Among authors: read ap. Trends Mol Med. 2005 Oct;11(10):449-55. doi: 10.1016/j.molmed.2005.08.001. Epub 2005 Sep 8. Trends Mol Med. 2005. PMID: 16153893 Review.

8

Coinheritance of two rare genodermatoses (Papillon-Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study.

Hewitt C, Wu CL, Hattab FN, Amin W, Ghaffar KA, Toomes C, Sloan P, Read AP, James JA, Thakker NS. Hewitt C, et al. Among authors: read ap. Br J Dermatol. 2004 Dec;151(6):1261-5. doi: 10.1111/j.1365-2133.2004.06237.x. Br J Dermatol. 2004. PMID: 15606524

9

Determination of sequence variation and haplotype structure for the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes: investigation of role in pubertal timing.

Sedlmeyer IL, Pearce CL, Trueman JA, Butler JL, Bersaglieri T, Read AP, Clayton PE, Kolonel LN, Henderson BE, Hirschhorn JN, Palmert MR. Sedlmeyer IL, et al. Among authors: read ap. J Clin Endocrinol Metab. 2005 Feb;90(2):1091-9. doi: 10.1210/jc.2004-0649. Epub 2004 Nov 16. J Clin Endocrinol Metab. 2005. PMID: 15546906

10

DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinoma.

Hewitt C, Wilson P, McGlinn E, MacFarlane G, Papageorgiou A, Woodwards RT, Sloan P, Gollin SM, Paterson I, Parkinson KK, Read AP, Thakker N. Hewitt C, et al. Among authors: read ap. Cancer Lett. 2004 Jun 25;209(2):207-13. doi: 10.1016/j.canlet.2003.12.018. Cancer Lett. 2004. PMID: 15159023

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