Lensch MW - Search Results

1

Analysis of the CMT1A-REP repeat: mapping crossover breakpoints in CMT1A and HNPP.

Kiyosawa H, Lensch MW, Chance PF. Kiyosawa H, et al. Among authors: lensch mw. Hum Mol Genet. 1995 Dec;4(12):2327-34. doi: 10.1093/hmg/4.12.2327. Hum Mol Genet. 1995. PMID: 8634706

2

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17.

Chance PF, Abbas N, Lensch MW, Pentao L, Roa BB, Patel PI, Lupski JR. Chance PF, et al. Among authors: lensch mw. Hum Mol Genet. 1994 Feb;3(2):223-8. doi: 10.1093/hmg/3.2.223. Hum Mol Genet. 1994. PMID: 8004087

3

Connexin mutations in X-linked Charcot-Marie-Tooth disease.

Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH. Bergoffen J, et al. Among authors: lensch mw. Science. 1993 Dec 24;262(5142):2039-42. doi: 10.1126/science.8266101. Science. 1993. PMID: 8266101

4

Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A.

Chance PF, Bird TD, Matsunami N, Lensch MW, Brothman AR, Feldman GM. Chance PF, et al. Among authors: lensch mw. Neurology. 1992 Dec;42(12):2295-9. doi: 10.1212/wnl.42.12.2295. Neurology. 1992. PMID: 1461382

5

New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease.

Bone LJ, Dahl N, Lensch MW, Chance PF, Kelly T, Le Guern E, Magi S, Parry G, Shapiro H, Wang S, et al. Bone LJ, et al. Among authors: lensch mw. Neurology. 1995 Oct;45(10):1863-6. doi: 10.1212/wnl.45.10.1863. Neurology. 1995. PMID: 7477983

6

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders.

Chance PF, Lensch MW, Lipe H, Brown RH Sr, Brown RH Jr, Bird TD. Chance PF, et al. Among authors: lensch mw. Neurology. 1994 Dec;44(12):2253-7. doi: 10.1212/wnl.44.12.2253. Neurology. 1994. PMID: 7991108

7

Clinical and molecular analysis in Joubert syndrome.

Pellegrino JE, Lensch MW, Muenke M, Chance PF. Pellegrino JE, et al. Among authors: lensch mw. Am J Med Genet. 1997 Oct 3;72(1):59-62. doi: 10.1002/(sici)1096-8628(19971003)72:1<59::aid-ajmg12>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9295076

8

Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A.

Graf WD, Chance PF, Lensch MW, Eng LJ, Lipe HP, Bird TD. Graf WD, et al. Among authors: lensch mw. Cancer. 1996 Apr 1;77(7):1356-62. doi: 10.1002/(SICI)1097-0142(19960401)77:7<1356::AID-CNCR20>3.0.CO;2-#. Cancer. 1996. PMID: 8608515

9

DNA deletion associated with hereditary neuropathy with liability to pressure palsies.

Chance PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, Bird TD. Chance PF, et al. Among authors: lensch mw. Cell. 1993 Jan 15;72(1):143-51. doi: 10.1016/0092-8674(93)90058-x. Cell. 1993. PMID: 8422677

10

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

Matsunami N, Smith B, Ballard L, Lensch MW, Robertson M, Albertsen H, Hanemann CO, Müller HW, Bird TD, White R, et al. Matsunami N, et al. Among authors: lensch mw. Nat Genet. 1992 Jun;1(3):176-9. doi: 10.1038/ng0692-176. Nat Genet. 1992. PMID: 1303231

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