Hart KA - Search Results

1

Pathogenic and nonpathogenic deletions in two families with Duchenne muscular dystrophy.

Hart KA, Abbs S, Bobrow M. Hart KA, et al. Am J Med Genet. 1989 May;33(1):142-5. doi: 10.1002/ajmg.1320330123. Am J Med Genet. 1989. PMID: 2750784

2

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.

Hodgson S, Hart K, Abbs S, Heckmatt J, Rodillo E, Bobrow M, Dubowitz V. Hodgson S, et al. J Med Genet. 1989 Nov;26(11):682-93. doi: 10.1136/jmg.26.11.682. J Med Genet. 1989. PMID: 2585468 Free PMC article.

3

Linkage studies in Duchenne and Becker muscular dystrophies.

Walker A, Hart K, Cole C, Hodgson S, Johnson L, Dubowitz V, Bobrow M. Walker A, et al. J Med Genet. 1986 Dec;23(6):538-47. doi: 10.1136/jmg.23.6.538. J Med Genet. 1986. PMID: 2879925 Free PMC article.

4

The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.

Hodgson S, Walker A, Cole C, Hart K, Johnson L, Heckmatt J, Dubowitz V, Bobrow M. Hodgson S, et al. J Med Genet. 1987 Mar;24(3):152-9. doi: 10.1136/jmg.24.3.152. J Med Genet. 1987. PMID: 3572997 Free PMC article.

5

The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.

Hart K, Cole C, Walker A, Hodgson S, Johnson L, Dubowitz V, Ray P, Worton R, Bobrow M. Hart K, et al. J Med Genet. 1986 Dec;23(6):516-20. doi: 10.1136/jmg.23.6.516. J Med Genet. 1986. PMID: 3806637 Free PMC article.

6

Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy.

Roberts RG, Cole CG, Hart KA, Bobrow M, Bentley DR. Roberts RG, et al. Among authors: hart ka. Nucleic Acids Res. 1989 Jan 25;17(2):811. doi: 10.1093/nar/17.2.811. Nucleic Acids Res. 1989. PMID: 2563578 Free PMC article.

7

Molecular deletions in the Duchenne/Becker muscular dystrophy gene.

Hart KA, Abbs S, Wapenaar MC, Cole CG, Hodgson SV, Bobrow M. Hart KA, et al. Clin Genet. 1989 Apr;35(4):251-60. doi: 10.1111/j.1399-0004.1989.tb02939.x. Clin Genet. 1989. PMID: 2653672 Review.

8

Prenatal testing for Duchenne and Becker muscular dystrophy.

Cole CG, Walker A, Coyne A, Johnson L, Hart KA, Hodgson S, Sheridan R, Bobrow M. Cole CG, et al. Among authors: hart ka. Lancet. 1988 Feb 6;1(8580):262-6. doi: 10.1016/s0140-6736(88)90349-2. Lancet. 1988. PMID: 2893082

9

DNA deletions in mild and severe Becker muscular dystrophy.

Hart KA, Hodgson S, Walker A, Cole CG, Johnson L, Dubowitz V, Bobrow M. Hart KA, et al. Hum Genet. 1987 Mar;75(3):281-5. doi: 10.1007/BF00281075. Hum Genet. 1987. PMID: 3030926

10

A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region?

Hart KA, Monaco AP, Kunkel LM, Bobrow M. Hart KA, et al. Hum Genet. 1987 Sep;77(1):88-91. doi: 10.1007/BF00284721. Hum Genet. 1987. PMID: 3040577

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