Wallace MR - Search Results

1

Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.

Rasmussen SA, Colman SD, Ho VT, Abernathy CR, Arn PH, Weiss L, Schwartz C, Saul RA, Wallace MR. Rasmussen SA, et al. Among authors: wallace mr. J Med Genet. 1998 Jun;35(6):468-71. doi: 10.1136/jmg.35.6.468. J Med Genet. 1998. PMID: 9643287 Free PMC article.

2

Two NF1 mutations: frameshift in the GAP-related domain, and loss of two codons toward the 3' end of the gene.

Abernathy CR, Colman SD, Kousseff BG, Wallace MR. Abernathy CR, et al. Among authors: wallace mr. Hum Mutat. 1994;3(4):347-52. doi: 10.1002/humu.1380030404. Hum Mutat. 1994. PMID: 8081387

3

Characterization of a single base-pair deletion in neurofibromatosis type 1.

Colman SD, Collins FS, Wallace MR. Colman SD, et al. Among authors: wallace mr. Hum Mol Genet. 1993 Oct;2(10):1709-11. doi: 10.1093/hmg/2.10.1709. Hum Mol Genet. 1993. PMID: 8268926

4

Somatic mosaicism in a patient with neurofibromatosis type 1.

Colman SD, Rasmussen SA, Ho VT, Abernathy CR, Wallace MR. Colman SD, et al. Among authors: wallace mr. Am J Hum Genet. 1996 Mar;58(3):484-90. Am J Hum Genet. 1996. PMID: 8644707 Free PMC article.

5

A multiplex-PCR test for EVI2A and EVI2B polymorphisms within the human NF1 gene.

Rasmussen SA, Ho VT, Colman SD, Abernathy CR, Wallace MR. Rasmussen SA, et al. Among authors: wallace mr. Mamm Genome. 1996 Mar;7(3):233-4. doi: 10.1007/s003359900065. Mamm Genome. 1996. PMID: 8833251 No abstract available.

6

NF1 mutation analysis using a combined heteroduplex/SSCP approach.

Abernathy CR, Rasmussen SA, Stalker HJ, Zori R, Driscoll DJ, Williams CA, Kousseff BG, Wallace MR. Abernathy CR, et al. Among authors: wallace mr. Hum Mutat. 1997;9(6):548-54. doi: 10.1002/(SICI)1098-1004(1997)9:6<548::AID-HUMU8>3.0.CO;2-Y. Hum Mutat. 1997. PMID: 9195229

7

Four frameshift mutations in neurofibromatosis type 1 caused by small insertions.

Colman SD, Abernathy CR, Ho VT, Wallace MR. Colman SD, et al. Among authors: wallace mr. J Med Genet. 1997 Jul;34(7):579-81. doi: 10.1136/jmg.34.7.579. J Med Genet. 1997. PMID: 9222967 Free PMC article.

8

A new hereditary cylindromatosis family associated with CYLD1 on chromosome 16.

Thomson SA, Rasmussen SA, Zhang J, Wallace MR. Thomson SA, et al. Among authors: wallace mr. Hum Genet. 1999 Jul-Aug;105(1-2):171-3. doi: 10.1007/s004399900077. Hum Genet. 1999. PMID: 10480375

9

Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene.

Colman SD, Williams CA, Wallace MR. Colman SD, et al. Among authors: wallace mr. Nat Genet. 1995 Sep;11(1):90-2. doi: 10.1038/ng0995-90. Nat Genet. 1995. PMID: 7550323

10

Neurofibromatosis type 1.

Colman SD, Wallace MR. Colman SD, et al. Among authors: wallace mr. Eur J Cancer. 1994;30A(13):1974-81. doi: 10.1016/0959-8049(94)00389-m. Eur J Cancer. 1994. PMID: 7734210 Review. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

369 results

Search Page

Filters