Huson SM - Search Results

1

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.

Meredith AL, Huson SM, Lunt PW, Sarfarazi M, Harley HG, Brook JD, Shaw DJ, Harper PS. Meredith AL, et al. Among authors: huson sm. Br Med J (Clin Res Ed). 1986 Nov 22;293(6558):1353-6. doi: 10.1136/bmj.293.6558.1353. Br Med J (Clin Res Ed). 1986. PMID: 2878705 Free PMC article.

2

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: huson sm. Hum Genet. 1986 Nov;74(3):262-6. doi: 10.1007/BF00282545. Hum Genet. 1986. PMID: 2877933

3

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: huson sm. Hum Genet. 1986 Nov;74(3):267-9. doi: 10.1007/BF00282546. Hum Genet. 1986. PMID: 2877934

4

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: huson sm. Hum Genet. 1985;70(3):271-3. doi: 10.1007/BF00273455. Hum Genet. 1985. PMID: 2991117

5

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. 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.

6

Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1.

Upadhyaya M, Fryer A, MacMillan J, Broadhead W, Huson SM, Harper PS. Upadhyaya M, et al. Among authors: huson sm. J Med Genet. 1992 Mar;29(3):180-3. doi: 10.1136/jmg.29.3.180. J Med Genet. 1992. PMID: 1348093 Free PMC article.

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. 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

An exclusion map for Von Recklinghausen neurofibromatosis.

Sarfarazi M, Huson SM, Edwards JH. Sarfarazi M, et al. Among authors: huson sm. J Med Genet. 1987 Sep;24(9):515-20. doi: 10.1136/jmg.24.9.515. J Med Genet. 1987. PMID: 3118026 Free PMC article.

9

Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.

Upadhyaya M, Sarfarazi M, Huson SM, Harper PS. Upadhyaya M, et al. Among authors: huson sm. J Med Genet. 1987 Sep;24(9):534-6. doi: 10.1136/jmg.24.9.534. J Med Genet. 1987. PMID: 3118035 Free PMC article.

10

A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.

Huson SM, Compston DA, Harper PS. Huson SM, et al. J Med Genet. 1989 Nov;26(11):712-21. doi: 10.1136/jmg.26.11.712. J Med Genet. 1989. PMID: 2511319 Free PMC article. Review.

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