Búsqueda | Biblioteca Virtual en Salud

1.

Inherited eye disease: cause and late effect.

Manson, Forbes D C; Trump, Dorothy; Read, Andrew P; Black, Graeme C M.

Trends Mol Med ; 11(10): 449-55, 2005 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-16153893

2.

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

Banerjee, Indraneel; Trueman, Julie A; Hall, Catherine M; Price, David A; Patel, Leena; Whatmore, Andrew J; Hirschhorn, Joel N; Read, Andrew P; Palmert, Mark R; Clayton, Peter E.

Eur J Endocrinol ; 155(1): 121-6, 2006 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-16793957

3.

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

Sedlmeyer, Ines L; Pearce, Celeste Leigh; Trueman, Julie A; Butler, Johannah L; Bersaglieri, Todd; Read, Andrew P; Clayton, Peter E; Kolonel, Laurence N; Henderson, Brian E; Hirschhorn, Joel N; Palmert, Mark R.

J Clin Endocrinol Metab ; 90(2): 1091-9, 2005 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-15546906

4.

How clinicians add to knowledge of development.

Donnai, Dian; Read, Andrew P.

Lancet ; 362(9382): 477-84, 2003 Aug 09.

Artículo en Inglés | MEDLINE | ID: mdl-12927438

5.

The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis.

Hewitt, Chelsee; McCormick, Derek; Linden, Gerry; Turk, Dusan; Stern, Igor; Wallace, Ian; Southern, Louise; Zhang, Liqun; Howard, Rebecca; Bullon, Pedro; Wong, Melanie; Widmer, Richard; Gaffar, Khaled Abdul; Awawdeh, Lama; Briggs, Jim; Yaghmai, Reza; Jabs, Ethlin W; Hoeger, Peter; Bleck, Oliver; Rüdiger, Stefan G; Petersilka, Gregor; Battino, Maurizio; Brett, Peter; Hattab, Faiez; Al-Hamed, Mohamed; Sloan, Philip; Toomes, Carmel; Dixon, Mike; James, Jacqueline; Read, Andrew P; Thakker, Nalin.

Hum Mutat ; 23(3): 222-8, 2004 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-14974080

6.

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

Hewitt, Chelsee; Wilson, Peter; McGlinn, Edwina; MacFarlane, Gary; Papageorgiou, Anne; Woodwards, Robert T M; Sloan, Philip; Gollin, Susanne M; Paterson, Ian; Parkinson, Kenneth K; Read, Andrew P; Thakker, Nalin.

Cancer Lett ; 209(2): 207-13, 2004 Jun 25.

Artículo en Inglés | MEDLINE | ID: mdl-15159023

7.

Read's Recall: Shuffling abstracts - and foundations.

Read, Andrew P.

Eur J Hum Genet ; 25(s2): S27-S28, 2017 12.

Artículo en Inglés | MEDLINE | ID: mdl-29297877

8.

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

Read, Andrew P; Donnai, Dian.

J Community Genet ; 3(3): 167-74, 2012 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-22760671

9.

GTF2IRD1 in craniofacial development of humans and mice.

Tassabehji, May; Hammond, Peter; Karmiloff-Smith, Annette; Thompson, Pamela; Thorgeirsson, Snorri S; Durkin, Marian E; Popescu, Nicholas C; Hutton, Timothy; Metcalfe, Kay; Rucka, Agnes; Stewart, Helen; Read, Andrew P; Maconochie, Mark; Donnai, Dian.

Science ; 310(5751): 1184-7, 2005 Nov 18.

Artículo en Inglés | MEDLINE | ID: mdl-16293761

10.

SLUG (SNAI2) deletions in patients with Waardenburg disease.

Sánchez-Martín, Manuel; Rodríguez-García, Arancha; Pérez-Losada, Jesús; Sagrera, Ana; Read, Andrew P; Sánchez-García, Isidro.

Hum Mol Genet ; 11(25): 3231-6, 2002 Dec 01.

Artículo en Inglés | MEDLINE | ID: mdl-12444107

11.

Germline mutation of ARF in a melanoma kindred.

Hewitt, Chelsee; Lee Wu, Chu; Evans, Gareth; Howell, A; Elles, Robert G; Jordan, Richard; Sloan, Philip; Read, Andrew P; Thakker, Nalin.

Hum Mol Genet ; 11(11): 1273-9, 2002 May 15.

Artículo en Inglés | MEDLINE | ID: mdl-12019208

12.

Genética molecular humana / Human molecular genetics

Strachan, Tom; Read, Andrew P.

Porto Alegre; Artmed; 2ed; 2002. iv,576 p. ilus.

Monografía en Portugués | BVSDIP, FIOCRUZ | ID: dip-804

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