Flintoff W - Search Results

1

Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.

Edery P, Pelet A, Mulligan LM, Abel L, Attié T, Dow E, Bonneau D, David A, Flintoff W, Jan D, et al. Edery P, et al. Among authors: flintoff w. J Med Genet. 1994 Aug;31(8):602-6. doi: 10.1136/jmg.31.8.602. J Med Genet. 1994. PMID: 7815416 Free PMC article.

2

No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome families.

Flintoff WF, Bahuau M, Lyonnet S, Gilgenkrantz S, Lacombe D, Marçon F, Levilliers J, Kachaner J, Munnich A, Le Merrer M. Flintoff WF, et al. Am J Med Genet. 1993 Jul 1;46(6):700-5. doi: 10.1002/ajmg.1320460621. Am J Med Genet. 1993. PMID: 8362913

3

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.

Bahuau M, Flintoff W, Assouline B, Lyonnet S, Le Merrer M, Prieur M, Guilloud-Bataille M, Feingold N, Munnich A, Vidaud M, Vidaud D. Bahuau M, et al. Among authors: flintoff w. Am J Med Genet. 1996 Dec 18;66(3):347-55. doi: 10.1002/(SICI)1096-8628(19961218)66:3<347::AID-AJMG20>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8985499

4

Choroideremia associated with an X-autosomal translocation.

Siu VM, Gonder JR, Jung JH, Sergovich FR, Flintoff WF. Siu VM, et al. Among authors: flintoff wf. Hum Genet. 1990 Apr;84(5):459-64. doi: 10.1007/BF00195820. Hum Genet. 1990. PMID: 2323779 Free PMC article.

5

DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation.

Merry DE, Lesko JG, Siu V, Flintoff WF, Collins F, Lewis RA, Nussbaum RL. Merry DE, et al. Among authors: flintoff wf. Genomics. 1990 Apr;6(4):609-15. doi: 10.1016/0888-7543(90)90494-f. Genomics. 1990. PMID: 2341150 Free article.

6

Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

Cremers FP, van de Pol DJ, Wieringa B, Collins FS, Sankila EM, Siu VM, Flintoff WF, Brunsmann F, Blonden LA, Ropers HH. Cremers FP, et al. Among authors: flintoff wf. Proc Natl Acad Sci U S A. 1989 Oct;86(19):7510-4. doi: 10.1073/pnas.86.19.7510. Proc Natl Acad Sci U S A. 1989. PMID: 2798422 Free PMC article.

7

Chromosomal localization of the reduced folate transporter gene (SLC19A1) in Chinese hamster ovary cells.

Chan FP, Williams FM, Rogers KA, Flintoff WF. Chan FP, et al. Among authors: flintoff wf. Cytogenet Cell Genet. 1995;71(2):148-50. doi: 10.1159/000134095. Cytogenet Cell Genet. 1995. PMID: 7656585 No abstract available.

8

Molecular cloning of a gene involved in methotrexate uptake by DNA-mediated gene transfer.

Underhill TM, Williams FM, Murray RC, Flintoff WF. Underhill TM, et al. Among authors: flintoff wf. Somat Cell Mol Genet. 1992 Jul;18(4):337-49. doi: 10.1007/BF01235757. Somat Cell Mol Genet. 1992. PMID: 1440056

9

Complementation of a methotrexate uptake defect in Chinese hamster ovary cells by DNA-mediated gene transfer.

Underhill TM, Flintoff WF. Underhill TM, et al. Among authors: flintoff wf. Mol Cell Biol. 1989 Apr;9(4):1754-8. doi: 10.1128/mcb.9.4.1754-1758.1989. Mol Cell Biol. 1989. PMID: 2725523 Free PMC article.

10

Mutant Chinese hamster ovary cells with defective methotrexate uptake are distinguishable by reversion analysis.

Underhill TM, Flintoff WF. Underhill TM, et al. Among authors: flintoff wf. Somat Cell Mol Genet. 1989 Jan;15(1):49-59. doi: 10.1007/BF01534669. Somat Cell Mol Genet. 1989. PMID: 2783789

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