Kingston HM - Search Results

1

Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy.

Brown CS, Thomas NS, Sarfarazi M, Davies KE, Kunkel L, Pearson PL, Kingston HM, Shaw DJ, Harper PS. Brown CS, et al. Among authors: kingston hm. Hum Genet. 1985;71(1):62-74. doi: 10.1007/BF00295671. Hum Genet. 1985. PMID: 2993158

2

Becker muscular dystrophy: correlation of deletion type with clinical severity.

Norman AM, Thomas NS, Kingston HM, Harper PS. Norman AM, et al. Among authors: kingston hm. J Med Genet. 1990 Apr;27(4):236-9. doi: 10.1136/jmg.27.4.236. J Med Genet. 1990. PMID: 2325103 Free PMC article.

3

Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis.

Kingston HM, Sarfarazi M, Newcombe RG, Willis N, Harper PS. Kingston HM, et al. Clin Genet. 1985 Apr;27(4):383-91. doi: 10.1111/j.1399-0004.1985.tb02280.x. Clin Genet. 1985. PMID: 3995787

4

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.

Kingston HM, Sarfarazi M, Thomas NS, Harper PS. Kingston HM, et al. Hum Genet. 1984;67(1):6-17. doi: 10.1007/BF00270551. Hum Genet. 1984. PMID: 6086495

5

Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy.

Sarfarazi M, Harper PS, Kingston HM, Murray JM, O'Brien T, Davies KE, Williamson R, Tippett P, Sanger R. Sarfarazi M, et al. Among authors: kingston hm. Hum Genet. 1983;65(2):169-71. doi: 10.1007/BF00286656. Hum Genet. 1983. PMID: 6317539

6

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.

Kingston HM, Thomas NS, Pearson PL, Sarfarazi M, Harper PS. Kingston HM, et al. J Med Genet. 1983 Aug;20(4):255-8. doi: 10.1136/jmg.20.4.255. J Med Genet. 1983. PMID: 6620324 Free PMC article.

7

Localisation of gene for Becker muscular dystrophy.

Kingston HM, Harper PS, Pearson PL, Davies KE, Williamson R, Page D. Kingston HM, et al. Lancet. 1983 Nov 19;2(8360):1200. doi: 10.1016/s0140-6736(83)91252-7. Lancet. 1983. PMID: 6139558 No abstract available.

8

An autosomal dominant syndrome of uveal colobomata, cleft lip and palate, and mental retardation.

Kingston HM, Harper PS, Jones PW. Kingston HM, et al. J Med Genet. 1982 Dec;19(6):444-6. doi: 10.1136/jmg.19.6.444. J Med Genet. 1982. PMID: 7154042 Free PMC article.

9

Prenatal diagnosis of Hunter syndrome.

Archer IM, Kingston HM, Harper PS. Archer IM, et al. Among authors: kingston hm. Prenat Diagn. 1984 May-Jun;4(3):195-200. doi: 10.1002/pd.1970040306. Prenat Diagn. 1984. PMID: 6431402

10

Orocraniodigital (Juberg-Hayward) syndrome with growth hormone deficiency.

Kingston HM, Hughes IA, Harper PS. Kingston HM, et al. Arch Dis Child. 1982 Oct;57(10):790-2. doi: 10.1136/adc.57.10.790. Arch Dis Child. 1982. PMID: 7138070 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

146 results

Search Page