White MB - Search Results

1

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients.

Dean M, White MB, Amos J, Gerrard B, Stewart C, Khaw KT, Leppert M. Dean M, et al. Among authors: white mb. Cell. 1990 Jun 1;61(5):863-70. doi: 10.1016/0092-8674(90)90196-l. Cell. 1990. PMID: 2344617

2

A 22-bp deletion in the coding region of the cystic fibrosis gene.

Dean M, White MB, Gerrard B, Milunsky A, Amos J. Dean M, et al. Among authors: white mb. Genomics. 1992 May;13(1):235-6. doi: 10.1016/0888-7543(92)90233-i. Genomics. 1992. PMID: 1374361 No abstract available.

3

A frame-shift mutation in the cystic fibrosis gene.

White MB, Amos J, Hsu JM, Gerrard B, Finn P, Dean M. White MB, et al. Nature. 1990 Apr 12;344(6267):665-7. doi: 10.1038/344665a0. Nature. 1990. PMID: 1691449

4

Typing of HLA-DQA1 and DQB1 using DNA single-strand conformation polymorphism.

Carrington M, Miller T, White M, Gerrard B, Stewart C, Dean M, Mann D. Carrington M, et al. Hum Immunol. 1992 Mar;33(3):208-12. doi: 10.1016/0198-8859(92)90073-v. Hum Immunol. 1992. PMID: 1618658

5

Identification of P-glycoprotein/multidrug resistance genes from model organisms.

Allikmets R, Gerrard B, Stewart C, White M, Dean M. Allikmets R, et al. Leukemia. 1993 Aug;7 Suppl 2:S13-7. Leukemia. 1993. PMID: 8361216

6

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis.

Anguiano A, Oates RD, Amos JA, Dean M, Gerrard B, Stewart C, Maher TA, White MB, Milunsky A. Anguiano A, et al. Among authors: white mb. JAMA. 1992 Apr 1;267(13):1794-7. JAMA. 1992. PMID: 1545465

7

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT).

White MB, Krueger LJ, Holsclaw DS Jr, Gerrard BC, Stewart C, Quittell L, Dolganov G, Baranov V, Ivaschenko T, Kapronov NI, et al. White MB, et al. Genomics. 1991 May;10(1):266-9. doi: 10.1016/0888-7543(91)90510-l. Genomics. 1991. PMID: 1710600

8

A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR gene.

White MB, Leppert M, Nielsen D, Zielenski J, Gerrard B, Stewart C, Dean M. White MB, et al. Genomics. 1991 Nov;11(3):778-9. doi: 10.1016/0888-7543(91)90092-s. Genomics. 1991. PMID: 1723056 No abstract available.

9

Detecting single base substitutions as heteroduplex polymorphisms.

White MB, Carvalho M, Derse D, O'Brien SJ, Dean M. White MB, et al. Genomics. 1992 Feb;12(2):301-6. doi: 10.1016/0888-7543(92)90377-5. Genomics. 1992. PMID: 1740339

10

The use of DNA heteroduplex patterns to map recombination within the HLA class II region.

Carrington M, White MB, Dean M, Mann D, Ward FE. Carrington M, et al. Among authors: white mb. Hum Immunol. 1992 Feb;33(2):114-21. doi: 10.1016/0198-8859(92)90061-q. Hum Immunol. 1992. PMID: 1532959

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