Speer MC - Search Results

1

Familial inheritance of a DXS164 deletion mutation from a heterozygous female.

Lanman JT Jr, Pericak-Vance MA, Bartlett RJ, Chen JC, Yamaoka L, Koh J, Speer MC, Hung WY, Roses AD. Lanman JT Jr, et al. Among authors: speer mc. Am J Hum Genet. 1987 Aug;41(2):138-44. Am J Hum Genet. 1987. PMID: 2887110 Free PMC article.

2

Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I.

Vance JM, Pericak-Vance MA, Yamaoka LH, Speer MC, Rosenwasser GO, Small K, Gaskell PC Jr, Hung WY, Alberts MJ, Haynes CS, et al. Vance JM, et al. Among authors: speer mc. Am J Hum Genet. 1989 Jan;44(1):25-9. Am J Hum Genet. 1989. PMID: 2491777 Free PMC article.

3

Inherited deletion at Duchenne dystrophy locus in normal male.

Koh J, Bartlett RJ, Pericak-Vance MA, Speer MC, Yamaoka LH, Phillips K, Hung WY, Ray PN, Worton RG, Gilbert JR, et al. Koh J, et al. Among authors: speer mc. Lancet. 1987 Nov 14;2(8568):1154-5. doi: 10.1016/s0140-6736(87)91590-x. Lancet. 1987. PMID: 2890056 No abstract available.

4

Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy.

Speer MC, Pericak-Vance MA, Yamaoka LH, Koh J, Hung WY, Gaskell PC Jr, Vance JM, Bartlett RJ, Roses AD. Speer MC, et al. Prenat Diagn. 1988 Jul;8(6):427-37. doi: 10.1002/pd.1970080607. Prenat Diagn. 1988. PMID: 3211845

5

Duchenne muscular dystrophy: high frequency of deletions.

Bartlett RJ, Pericak-Vance MA, Koh J, Yamaoka LH, Chen JC, Hung WY, Speer MC, Wapenaar MC, Van Ommen GJ, Bakker E, et al. Bartlett RJ, et al. Among authors: speer mc. Neurology. 1988 Jan;38(1):1-4. doi: 10.1212/wnl.38.1.1. Neurology. 1988. PMID: 3275902

6

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C, et al. Hentati A, et al. Among authors: speer mc. Nat Genet. 1994 Jul;7(3):425-8. doi: 10.1038/ng0794-425. Nat Genet. 1994. PMID: 7920663

7

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

Messina DN, Speer MC, Pericak-Vance MA, McNally EM. Messina DN, et al. Among authors: speer mc. Am J Hum Genet. 1997 Oct;61(4):909-17. doi: 10.1086/514896. Am J Hum Genet. 1997. PMID: 9382102 Free PMC article.

8

Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy.

Falk CT, Gilchrist JM, Pericak-Vance MA, Speer MC. Falk CT, et al. Among authors: speer mc. Am J Hum Genet. 1998 Apr;62(4):941-9. doi: 10.1086/301780. Am J Hum Genet. 1998. PMID: 9529338 Free PMC article.

9

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Speer MC, Vance JM, Stewart CS, Yamaoka LH, Samson F, Fardeau M, Potter TG, Roses AD, et al. Gilbert JR, et al. Among authors: speer mc. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.

10

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

Speer MC, Yamaoka LH, Gilchrist JH, Gaskell CP, Stajich JM, Vance JM, Kazantsev A, Lastra AA, Haynes CS, Beckmann JS, et al. Speer MC, et al. Am J Hum Genet. 1992 Jun;50(6):1211-7. Am J Hum Genet. 1992. PMID: 1598902 Free PMC article.

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