Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

47 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Maternal uniparental heterodisomy for chromosome 16: case report.
Woo V, Bridge PJ, Bamforth JS. Woo V, et al. Among authors: bamforth js. Am J Med Genet. 1997 Jun 27;70(4):387-90. doi: 10.1002/(sici)1096-8628(19970627)70:4<387::aid-ajmg10>3.0.co;2-d. Am J Med Genet. 1997. PMID: 9182779
The different effects on cranial and trunk neural crest cell behaviour following exposure to a low concentration of alcohol in vitro.
Czarnobaj J, Bagnall KM, Bamforth JS, Milos NC. Czarnobaj J, et al. Among authors: bamforth js. Arch Oral Biol. 2014 May;59(5):500-12. doi: 10.1016/j.archoralbio.2014.02.005. Epub 2014 Feb 18. Arch Oral Biol. 2014. PMID: 24631632
Differential CRX and OTX2 expression in human retina and retinoblastoma.
Glubrecht DD, Kim JH, Russell L, Bamforth JS, Godbout R. Glubrecht DD, et al. Among authors: bamforth js. J Neurochem. 2009 Oct;111(1):250-63. doi: 10.1111/j.1471-4159.2009.06322.x. Epub 2009 Aug 3. J Neurochem. 2009. PMID: 19686387 Free PMC article.
Adams Oliver syndrome: a family with extreme variability in clinical expression.
Bamforth JS, Kaurah P, Byrne J, Ferreira P. Bamforth JS, et al. Am J Med Genet. 1994 Feb 15;49(4):393-6. doi: 10.1002/ajmg.1320490408. Am J Med Genet. 1994. PMID: 8160731
Lymphatic abnormalities in fetuses with posterior cervical cystic hygroma.
Chitayat D, Kalousek DK, Bamforth JS. Chitayat D, et al. Among authors: bamforth js. Am J Med Genet. 1989 Jul;33(3):352-6. doi: 10.1002/ajmg.1320330313. Am J Med Genet. 1989. PMID: 2801770
Genetic study of SOX9 in a case of campomelic dysplasia.
Giordano J, Prior HM, Bamforth JS, Walter MA. Giordano J, et al. Among authors: bamforth js. Am J Med Genet. 2001 Jan 15;98(2):176-81. doi: 10.1002/1096-8628(20010115)98:2<176::aid-ajmg1027>3.0.co;2-q. Am J Med Genet. 2001. PMID: 11223854
Soft tissue facial resemblance in families and syndrome-affected individuals.
Shaner DJ, Peterson AE, Beattie OB, Bamforth JS. Shaner DJ, et al. Among authors: bamforth js. Am J Med Genet. 2001 Sep 1;102(4):330-41. doi: 10.1002/ajmg.1491. Am J Med Genet. 2001. PMID: 11503160
Assessment of soft tissue facial asymmetry in medically normal and syndrome-affected individuals by analysis of landmarks and measurements.
Shaner DJ, Peterson AE, Beattie OB, Bamforth JS. Shaner DJ, et al. Among authors: bamforth js. Am J Med Genet. 2000 Jul 17;93(2):143-54. doi: 10.1002/1096-8628(20000717)93:2<143::aid-ajmg12>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10869118
Facial measurements in clinical genetics: How important are the instruments we use?
Shaner DJ, Peterson AE, Beattie OB, Bamforth JS. Shaner DJ, et al. Among authors: bamforth js. Am J Med Genet. 1998 Jun 5;77(5):384-90. doi: 10.1002/(sici)1096-8628(19980605)77:5<384::aid-ajmg6>3.0.co;2-n. Am J Med Genet. 1998. PMID: 9632167
DK phocomelia phenotype (von Voss-Cherstvoy syndrome) caused by somatic mosaicism for del(13q).
Bamforth JS, Lin CC. Bamforth JS, et al. Am J Med Genet. 1997 Dec 31;73(4):408-11. Am J Med Genet. 1997. PMID: 9415466 Review.
47 results
Jump to page
Feedback