Mathews KD - Search Results

1

Reed PW, Mathews KD, Mills KA, Bloch RJ. Reed PW, et al. Among authors: mathews kd. Muscle Nerve. 2004 Nov;30(5):585-95. doi: 10.1002/mus.20146. Muscle Nerve. 2004. PMID: 15389724

2

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC. Mathews KD, et al. Am J Hum Genet. 1992 Aug;51(2):428-31. Am J Hum Genet. 1992. PMID: 1642242 Free PMC article.

3

Genetic mapping near the myd locus on mouse chromosome 8.

Mills KA, Mathews KD, Scherpbier-Heddema T, Schelper RL, Schmalzel R, Bailey HL, Nadeau JH, Buetow KH, Murray JC. Mills KA, et al. Among authors: mathews kd. Mamm Genome. 1995 Apr;6(4):278-80. doi: 10.1007/BF00352416. Mamm Genome. 1995. PMID: 7613034

4

Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.

Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC. Mathews KD, et al. Muscle Nerve Suppl. 1995;2:S98-102. Muscle Nerve Suppl. 1995. PMID: 7739634

5

A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.

Mills KA, Sunada Y, Campbell KP, Mathews KD. Mills KA, et al. Among authors: mathews kd. Mamm Genome. 1995 Sep;6(9):664-5. doi: 10.1007/BF00352377. Mamm Genome. 1995. PMID: 8535078 No abstract available.

6

The Ant1 gene maps near Klk3 on proximal mouse chromosome 8.

Mills KA, Ellison JW, Mathews KD. Mills KA, et al. Among authors: mathews kd. Mamm Genome. 1996 Sep;7(9):707. doi: 10.1007/s003359900296. Mamm Genome. 1996. PMID: 8703133 No abstract available.

7

Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8.

Mills KA, Mathews KD, Scherpbier-Heddema T, Buetow KH, Baldini A, Ballabio A, Borsani G. Mills KA, et al. Among authors: mathews kd. Genomics. 1996 Sep 1;36(2):374-6. doi: 10.1006/geno.1996.0480. Genomics. 1996. PMID: 8812471 No abstract available.

8

The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse model.

Mathews KD, Mills KA. Mathews KD, et al. Curr Opin Neurol. 1996 Oct;9(5):394-9. Curr Opin Neurol. 1996. PMID: 8894417 Review.

9

The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.

Grewal PK, van Deutekom JC, Mills KA, Lemmers RJ, Mathews KD, Frants RR, Hewitt JE. Grewal PK, et al. Among authors: mathews kd. Mamm Genome. 1997 Jun;8(6):394-8. doi: 10.1007/s003359900454. Mamm Genome. 1997. PMID: 9166581

10

Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.

Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC. Mathews KD, et al. Muscle Nerve Suppl. 1995;(2):S98-102. Muscle Nerve Suppl. 1995. PMID: 23573594

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