Lennon F - Search Results

1

A gene for familial venous malformations maps to chromosome 9p in a second large kindred.

Gallione CJ, Pasyk KA, Boon LM, Lennon F, Johnson DW, Helmbold EA, Markel DS, Vikkula M, Mulliken JB, Warman ML, et al. Gallione CJ, et al. Among authors: lennon f. J Med Genet. 1995 Mar;32(3):197-9. doi: 10.1136/jmg.32.3.197. J Med Genet. 1995. PMID: 7783168 Free PMC article.

2

Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.

McAllister KA, Lennon F, Bowles-Biesecker B, McKinnon WC, Helmbold EA, Markel DS, Jackson CE, Guttmacher AE, Pericak-Vance MA, Marchuk DA. McAllister KA, et al. Among authors: lennon f. J Med Genet. 1994 Dec;31(12):927-32. doi: 10.1136/jmg.31.12.927. J Med Genet. 1994. PMID: 7891374 Free PMC article.

3

Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia.

Speer MC, Kingston HM, Boustany RM, Gaskell PC, Robinson LC, Lennon F, Wolpert CM, Yamaoka LH, Kahler SG, Hogan EL, et al. Speer MC, et al. Among authors: lennon f. Am J Med Genet. 1995 Aug 14;60(4):307-11. doi: 10.1002/ajmg.1320600409. Am J Med Genet. 1995. PMID: 7485266

4

Linkage of a gene for macular corneal dystrophy to chromosome 16.

Vance JM, Jonasson F, Lennon F, Sarrica J, Damji KF, Stauffer J, Pericak-Vance MA, Klintworth GK. Vance JM, et al. Among authors: lennon f. Am J Hum Genet. 1996 Apr;58(4):757-62. Am J Hum Genet. 1996. PMID: 8644739 Free PMC article.

5

Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.

Scott WK, Gaskell PC, Lennon F, Wolpert CM, Menold MM, Aylsworth AS, Warner C, Farrell CD, Boustany RM, Albright SG, Boyd E, Kingston HM, Cumming WJ, Vance JM, Pericak-Vance MA. Scott WK, et al. Among authors: lennon f. Neurogenetics. 1997 Sep;1(2):95-102. doi: 10.1007/s100480050014. Neurogenetics. 1997. PMID: 10732810

6

Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation.

Stajich JM, Gilchrist JM, Lennon F, Lee A, Yamaoka L, Rosi B, Gaskell PC, Pritchard M, Donald L, Roses AD, Vance JM, Pericak-Vance MA. Stajich JM, et al. Among authors: lennon f. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S75-81. doi: 10.1016/s0960-8966(97)00087-4. Neuromuscul Disord. 1997. PMID: 9392021

7

Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.

Raskind WH, Pericak-Vance MA, Lennon F, Wolff J, Lipe HP, Bird TD. Raskind WH, et al. Among authors: lennon f. Am J Med Genet. 1997 Feb 21;74(1):26-36. doi: 10.1002/(sici)1096-8628(19970221)74:1<26::aid-ajmg7>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9034002

8

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM. Ben Othmane K, et al. Among authors: lennon f. Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625. Hum Mol Genet. 1993. PMID: 8268915

9

Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.

Ben Othmane K, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA, et al. Ben Othmane K, et al. Among authors: lennon f. Genomics. 1993 Aug;17(2):370-5. doi: 10.1006/geno.1993.1334. Genomics. 1993. PMID: 8406488

10

Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

Econs MJ, McEnery PT, Lennon F, Speer MC. Econs MJ, et al. Among authors: lennon f. J Clin Invest. 1997 Dec 1;100(11):2653-7. doi: 10.1172/JCI119809. J Clin Invest. 1997. PMID: 9389727 Free PMC article.

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