Meredith AL - Search Results

1

Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids.

Brook JD, Shaw DJ, Thomas NS, Meredith AL, Cowell J, Harper PS. Brook JD, et al. Among authors: meredith al. Cytogenet Cell Genet. 1986;41(1):30-7. doi: 10.1159/000132192. Cytogenet Cell Genet. 1986. PMID: 3455910

2

Gene mapping and chromosome 19.

Shaw DJ, Brook JD, Meredith AL, Harley HG, Sarfarazi M, Harper PS. Shaw DJ, et al. Among authors: meredith al. J Med Genet. 1986 Feb;23(1):2-10. doi: 10.1136/jmg.23.1.2. J Med Genet. 1986. PMID: 3081724 Free PMC article. Review.

3

Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.

Shaw DJ, Meredith AL, Sarfarazi M, Harley HG, Huson SM, Brook JD, Bufton L, Litt M, Mohandas T, Harper PS. Shaw DJ, et al. Among authors: meredith al. Hum Genet. 1986 Nov;74(3):262-6. doi: 10.1007/BF00282545. Hum Genet. 1986. PMID: 2877933

4

Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19.

Shaw DJ, Meredith AL, Brook JD, Sarfarzi M, Harley HG, Huson SM, Bell GI, Harper PS. Shaw DJ, et al. Among authors: meredith al. Hum Genet. 1986 Nov;74(3):267-9. doi: 10.1007/BF00282546. Hum Genet. 1986. PMID: 2877934

5

The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.

Shaw DJ, Meredith AL, Sarfarazi M, Huson SM, Brook JD, Myklebost O, Harper PS. Shaw DJ, et al. Among authors: meredith al. Hum Genet. 1985;70(3):271-3. doi: 10.1007/BF00273455. Hum Genet. 1985. PMID: 2991117

6

Myotonic dystrophy and gene mapping on human chromosome 19.

Brook JD, Shaw DJ, Meredith AL. Brook JD, et al. Among authors: meredith al. Biotechnol Genet Eng Rev. 1985;3:311-47. doi: 10.1080/02648725.1985.10647817. Biotechnol Genet Eng Rev. 1985. PMID: 3004536 Review. No abstract available.

7

Evidence against linkage of von Recklinghausen neurofibromatosis and chromosome 19 markers.

Huson SM, Meredith AL, Sarfarazi M, Shaw DJ, Brook D, Compston DA, Harper PS. Huson SM, et al. Among authors: meredith al. Ann N Y Acad Sci. 1986;486:349-53. doi: 10.1111/j.1749-6632.1986.tb48088.x. Ann N Y Acad Sci. 1986. PMID: 3105398

8

Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.

Huson SM, Meredith AL, Sarfarazi M, Shaw DJ, Compston DA, Harper PS. Huson SM, et al. Among authors: meredith al. J Med Genet. 1986 Feb;23(1):55-7. doi: 10.1136/jmg.23.1.55. J Med Genet. 1986. PMID: 3081725 Free PMC article.

9

Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.

Myring J, Meredith AL, Harley HG, Kohn G, Norbury G, Harper PS, Shaw DJ. Myring J, et al. Among authors: meredith al. J Med Genet. 1992 Nov;29(11):785-8. doi: 10.1136/jmg.29.11.785. J Med Genet. 1992. PMID: 1453427 Free PMC article.

10

Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers.

Norman AM, Floyd JL, Meredith AL, Harper PS. Norman AM, et al. Among authors: meredith al. J Med Genet. 1989 Dec;26(12):750-4. doi: 10.1136/jmg.26.12.750. J Med Genet. 1989. PMID: 2575669 Free PMC article.

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