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

Search Page

MyNCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

19 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
Gibbons RJ, Bachoo S, Picketts DJ, Aftimos S, Asenbauer B, Bergoffen J, Berry SA, Dahl N, Fryer A, Keppler K, Kurosawa K, Levin ML, Masuno M, Neri G, Pierpont ME, Slaney SF, Higgs DR. Gibbons RJ, et al. Among authors: Slaney SF. Nat Genet. 1997 Oct;17(2):146-8. doi: 10.1038/ng1097-146. Nat Genet. 1997. PMID: 9326931 No abstract available.
Exclusive paternal origin of new mutations in Apert syndrome.
Moloney DM, Slaney SF, Oldridge M, Wall SA, Sahlin P, Stenman G, Wilkie AO. Moloney DM, et al. Among authors: Slaney SF. Nat Genet. 1996 May;13(1):48-53. doi: 10.1038/ng0596-48. Nat Genet. 1996. PMID: 8673103
Congenital cervical spinal fusion: a study in Apert syndrome.
Thompson DN, Slaney SF, Hall CM, Shaw D, Jones BM, Hayward RD. Thompson DN, et al. Among authors: Slaney SF. Pediatr Neurosurg. 1996 Jul;25(1):20-7. doi: 10.1159/000121091. Pediatr Neurosurg. 1996. PMID: 9055330
Acromelic frontonasal dysostosis.
Slaney SF, Goodman FR, Eilers-Walsman BL, Hall BD, Williams DK, Young ID, Hayward RD, Jones BM, Christianson AL, Winter RM. Slaney SF, et al. Am J Med Genet. 1999 Mar 12;83(2):109-16. Am J Med Genet. 1999. PMID: 10190481 Review.
19 results
Jump to page