Bullen P - Search Results

1

Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung.

Lako M, Strachan T, Bullen P, Wilson DI, Robson SC, Lindsay S. Lako M, et al. Among authors: bullen p. Gene. 1998 Sep 28;219(1-2):101-10. doi: 10.1016/s0378-1119(98)00393-x. Gene. 1998. PMID: 9757009

2

A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain.

Lako M, Lindsay S, Bullen P, Wilson DI, Robson SC, Strachan T. Lako M, et al. Among authors: bullen p. Hum Mol Genet. 1998 May;7(5):813-22. doi: 10.1093/hmg/7.5.813. Hum Mol Genet. 1998. PMID: 9536085

3

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

Fougerousse F, Bullen P, Herasse M, Lindsay S, Richard I, Wilson D, Suel L, Durand M, Robson S, Abitbol M, Beckmann JS, Strachan T. Fougerousse F, et al. Among authors: bullen p. Hum Mol Genet. 2000 Jan 22;9(2):165-73. doi: 10.1093/hmg/9.2.165. Hum Mol Genet. 2000. PMID: 10607827

4

SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development.

Hanley NA, Hagan DM, Clement-Jones M, Ball SG, Strachan T, Salas-Cortés L, McElreavey K, Lindsay S, Robson S, Bullen P, Ostrer H, Wilson DI. Hanley NA, et al. Among authors: bullen p. Mech Dev. 2000 Mar 1;91(1-2):403-7. doi: 10.1016/s0925-4773(99)00307-x. Mech Dev. 2000. PMID: 10704874 Free article.

5

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.

Li QY, Newbury-Ecob RA, Terrett JA, Wilson DI, Curtis AR, Yi CH, Gebuhr T, Bullen PJ, Robson SC, Strachan T, Bonnet D, Lyonnet S, Young ID, Raeburn JA, Buckler AJ, Law DJ, Brook JD. Li QY, et al. Among authors: bullen pj. Nat Genet. 1997 Jan;15(1):21-9. doi: 10.1038/ng0197-21. Nat Genet. 1997. PMID: 8988164

6

Human post-implantation embryo collection: medical and surgical techniques.

Bullen PJ, Robson SC, Strachan T. Bullen PJ, et al. Early Hum Dev. 1998 Jul 10;51(3):213-21. doi: 10.1016/s0378-3782(97)00118-7. Early Hum Dev. 1998. PMID: 9692791

7

Investigation of the epidemiology and prenatal diagnosis of holoprosencephaly in the North of England.

Bullen PJ, Rankin JM, Robson SC. Bullen PJ, et al. Am J Obstet Gynecol. 2001 May;184(6):1256-62. doi: 10.1067/mob.2001.111071. Am J Obstet Gynecol. 2001. PMID: 11349198

8

Antenatal detection of cleft lip with or without cleft palate: incidence of associated chromosomal and structural anomalies.

Gillham JC, Anand S, Bullen PJ. Gillham JC, et al. Among authors: bullen pj. Ultrasound Obstet Gynecol. 2009 Oct;34(4):410-5. doi: 10.1002/uog.6447. Ultrasound Obstet Gynecol. 2009. PMID: 19790102 Free article.

9

Outcome in fetal lower urinary tract obstruction: a prospective registry study.

Morris RK, Middleton LJ, Malin GL, Quinlan-Jones E, Daniels J, Khan KS, Deeks J, Kilby MD; PLUTO Collaborative Group. Morris RK, et al. Ultrasound Obstet Gynecol. 2015 Oct;46(4):424-31. doi: 10.1002/uog.14808. Epub 2015 Aug 31. Ultrasound Obstet Gynecol. 2015. PMID: 25689128 Free article. Clinical Trial.

10

Osteocraniostenosis: a further case report documenting the antenatal findings.

Smith A, Mehta S, Bullen P, Clayton-Smith J. Smith A, et al. Among authors: bullen p. Clin Dysmorphol. 2007 Apr;16(2):117-120. doi: 10.1097/01.mcd.0000220619.78273.a5. Clin Dysmorphol. 2007. PMID: 17351358

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