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Results: 17

1.

Myopathia distalis tarda hereditaria; 249 examined cases in 72 pedigrees.

WELANDER L.

Acta Med Scand Suppl. 1951;265:1-124. No abstract available.

PMID:
14894174
[PubMed - indexed for MEDLINE]
2.

Sequential tests for the detection of linkage.

MORTON NE.

Am J Hum Genet. 1955 Sep;7(3):277-318. No abstract available.

PMID:
13258560
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Refined genetic localization for central core disease.

Mulley JC, Kozman HM, Phillips HA, Gedeon AK, McCure JA, Iles DE, Gregg RG, Hogan K, Couch FJ, MacLennan DH, et al.

Am J Hum Genet. 1993 Feb;52(2):398-405.

PMID:
8430700
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination events.

Weiffenbach B, Dubois J, Storvick D, Tawil R, Jacobsen SJ, Gilbert J, Wijmenga C, Mendell JR, Winokur S, Altherr MR, et al.

Nat Genet. 1993 Jun;4(2):165-9.

PMID:
8102297
[PubMed - indexed for MEDLINE]
5.

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation.

Nonaka I, Sunohara N, Ishiura S, Satoyoshi E.

J Neurol Sci. 1981 Jul;51(1):141-55.

PMID:
7252518
[PubMed - indexed for MEDLINE]
6.

A new type of hereditary distal myopathy with characteristic sarcoplasmic bodies and intermediate (skeletin) filaments.

Edström L, Thornell LE, Eriksson A.

J Neurol Sci. 1980 Aug;47(2):171-90.

PMID:
6251174
[PubMed - indexed for MEDLINE]
7.

Late onset hereditary distal myopathy.

Markesbery WR, Griggs RC, Leach RP, Lapham LW.

Neurology. 1974 Feb;24(2):127-34. No abstract available.

PMID:
4855680
[PubMed - indexed for MEDLINE]
8.

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Ott J.

Am J Hum Genet. 1974 Sep;26(5):588-97. No abstract available.

PMID:
4422075
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Exclusion mapping.

Edwards JH.

J Med Genet. 1987 Sep;24(9):539-43.

PMID:
3669048
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Two different forms of beta myosin heavy chain are expressed in human striated muscle.

Jandreski MA, Sole MJ, Liew CC.

Hum Genet. 1987 Oct;77(2):127-31.

PMID:
3653886
[PubMed - indexed for MEDLINE]
11.

Molecular cloning and chromosomal localization of a gene coding for human cardiac myosin heavy-chain.

Matsuoka R, Chambers A, Kimura M, Kanda N, Bruns G, Yoshida M, Takao A.

Am J Med Genet. 1988 Feb;29(2):369-76.

PMID:
3354609
[PubMed - indexed for MEDLINE]
12.

A simple salting out procedure for extracting DNA from human nucleated cells.

Miller SA, Dykes DD, Polesky HF.

Nucleic Acids Res. 1988 Feb 11;16(3):1215. No abstract available.

PMID:
3344216
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

A routine method for the establishment of permanent growing lymphoblastoid cell lines.

Neitzel H.

Hum Genet. 1986 Aug;73(4):320-6.

PMID:
3017841
[PubMed - indexed for MEDLINE]
14.

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Weber JL, May PE.

Am J Hum Genet. 1989 Mar;44(3):388-96.

PMID:
2916582
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Sarfarazi M, Upadhyaya M, Padberg G, Pericak-Vance M, Siddique T, Lucotte G, Lunt P.

J Med Genet. 1989 Aug;26(8):481-4.

PMID:
2769720
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

A second-generation linkage map of the human genome.

Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M.

Nature. 1992 Oct 29;359(6398):794-801.

PMID:
1436057
[PubMed - indexed for MEDLINE]
17.

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.

Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, Gruter AM, Hofker MH, Moerer P, Williamson R, et al.

Nat Genet. 1992 Sep;2(1):26-30.

PMID:
1363881
[PubMed - indexed for MEDLINE]

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