Dean M - Search Results

1

Applications of heteroduplex analysis for mutation detection in disease genes.

Glavac D, Dean M. Glavac D, et al. Among authors: dean m. Hum Mutat. 1995;6(4):281-7. doi: 10.1002/humu.1380060402. Hum Mutat. 1995. PMID: 8680402 Review.

2

Screening for CF mutations in adult cystic fibrosis patients with a directed and optimized SSCP strategy.

Ravnik-Glavac M, Glavac D, Chernick M, di Sant'Agnese P, Dean M. Ravnik-Glavac M, et al. Among authors: dean m. Hum Mutat. 1994;3(3):231-8. doi: 10.1002/humu.1380030309. Hum Mutat. 1994. PMID: 7517265

3

Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene.

Ravnik-Glavac M, Glavac D, Dean M. Ravnik-Glavac M, et al. Among authors: dean m. Hum Mol Genet. 1994 May;3(5):801-7. doi: 10.1093/hmg/3.5.801. Hum Mol Genet. 1994. PMID: 7521710

4

Single-stranded conformation polymorphism analysis of the CFTR gene in Slovenian cystic fibrosis patients: detection of mutations and sequence variations.

Ravnik-Glavac M, Glavac D, Komel R, Dean M. Ravnik-Glavac M, et al. Among authors: dean m. Hum Mutat. 1993;2(4):286-92. doi: 10.1002/humu.1380020408. Hum Mutat. 1993. PMID: 7691352

5

Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutations.

Glavac D, Dean M. Glavac D, et al. Among authors: dean m. Hum Mutat. 1993;2(5):404-14. doi: 10.1002/humu.1380020513. Hum Mutat. 1993. PMID: 8257994

6

Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens.

Ravnik-Glavac M, Dean M, Glavac D. Ravnik-Glavac M, et al. Among authors: dean m. Pflugers Arch. 2000;439(3 Suppl):R53-5. Pflugers Arch. 2000. PMID: 10653141

7

Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR gene in a patient with congenital bilateral absence of the vas deferens.

Ravnik-Glavac M, Dean M, Glavac D. Ravnik-Glavac M, et al. Among authors: dean m. Hum Hered. 2000 Sep-Oct;50(5):318-9. doi: 10.1159/000022934. Hum Hered. 2000. PMID: 10878476 No abstract available.

8

DHPLC screening of cystic fibrosis gene mutations.

Ravnik-Glavac M, Atkinson A, Glavac D, Dean M. Ravnik-Glavac M, et al. Among authors: dean m. Hum Mutat. 2002 Apr;19(4):374-83. doi: 10.1002/humu.10065. Hum Mutat. 2002. PMID: 11933191

9

Identification of a rare cystic fibrosis mutation (S4X) in a Slovenian population.

Glavac D, Ravnik-Glavac M, Dean M. Glavac D, et al. Among authors: dean m. Hum Mol Genet. 1993 Mar;2(3):315-6. doi: 10.1093/hmg/2.3.315. Hum Mol Genet. 1993. PMID: 7684643 No abstract available.

10

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype.

Chen F, Kishida T, Yao M, Hustad T, Glavac D, Dean M, Gnarra JR, Orcutt ML, Duh FM, Glenn G, et al. Chen F, et al. Among authors: dean m. Hum Mutat. 1995;5(1):66-75. doi: 10.1002/humu.1380050109. Hum Mutat. 1995. PMID: 7728151

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