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Items: 1 to 20 of 412

1.

Hereditary lymphedema: evidence for linkage and genetic heterogeneity.

Ferrell RE, Levinson KL, Esman JH, Kimak MA, Lawrence EC, Barmada MM, Finegold DN.

Hum Mol Genet. 1998 Dec;7(13):2073-8.

PMID:
9817924
2.

Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

Irrthum A, Karkkainen MJ, Devriendt K, Alitalo K, Vikkula M.

Am J Hum Genet. 2000 Aug;67(2):295-301.

3.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
4.

Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.

Barr CL, Best L, Weksberg R.

Am J Med Genet. 2001 Nov 22;104(2):120-6.

PMID:
11746041
5.

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

Prakash S, Chung KW, Sinha S, Barmada M, Ellis D, Ferrell RE, Finegold DN, Randhawa PS, Dinda A, Vats A.

J Am Soc Nephrol. 2003 Jul;14(7):1794-803.

6.
7.

Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.

Ye X, Shi L, Yin W, Meng L, Wang QK, Bian Z.

J Clin Periodontol. 2009 Aug;36(8):627-33. doi: 10.1111/j.1600-051X.2009.01438.x.

PMID:
19552635
8.

Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.

Hocking LJ, Herbert CA, Nicholls RK, Williams F, Bennett ST, Cundy T, Nicholson GC, Wuyts W, Van Hul W, Ralston SH.

Am J Hum Genet. 2001 Nov;69(5):1055-61.

9.

Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.

Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Jones R, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany RM, Vance JM, Scott WK, Pericak-Vance MA.

Neurogenetics. 2001 Mar;3(2):91-7.

PMID:
11354831
10.

Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14.

Guo D, Hasham S, Kuang SQ, Vaughan CJ, Boerwinkle E, Chen H, Abuelo D, Dietz HC, Basson CT, Shete SS, Milewicz DM.

Circulation. 2001 May 22;103(20):2461-8.

11.

Age of onset in hereditary lymphedema.

Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN.

J Pediatr. 2003 Jun;142(6):704-8.

PMID:
12838201
12.

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.

Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A; French Research Network on FTD/FTD-MND..

Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c.

PMID:
19433740
13.

[The human major histocompatibility complex region is not a major susceptibility locus for Graves disease among the Hans in north of China].

Jin Y, Hu F, Teng W, Ben S, Zhang J, Xiong X, Huang W.

Zhonghua Yi Xue Za Zhi. 2002 Sep 25;82(18):1242-4. Chinese.

PMID:
12425802
14.

Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

Towbin JA, Li H, Taggart RT, Lehmann MH, Schwartz PJ, Satler CA, Ayyagari R, Robinson JL, Moss A, Hejtmancik JF.

Circulation. 1994 Dec;90(6):2635-44.

PMID:
7994803
15.

Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity.

Braig DU, Schäffer AA, Glocker E, Salzer U, Warnatz K, Peter HH, Grimbacher B.

Hum Genet. 2003 Apr;112(4):369-78.

PMID:
12574940
16.

Genome-wide scan identifies a susceptibility locus for familial primary cutaneous amyloidosis on chromosome 5p13.1-q11.2.

Lee DD, Lin MW, Chen IC, Huang CY, Liu MT, Wang CR, Chang YT, Liu HN, Liu TT, Wong CK, Tsai SF.

Br J Dermatol. 2006 Dec;155(6):1201-8.

PMID:
17107390
17.

Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity.

Pericak-Vance MA, Speer MC, Lennon F, West SG, Menold MM, Stajich JM, Wolpert CM, Slotterbeck BD, Saito M, Tim RW, Rozear MP, Middleton LT, Tsuji S, Vance JM.

Neurogenetics. 1997 Sep;1(2):89-93.

PMID:
10732809
18.

Mapping of primary congenital lymphedema to the 5q35.3 region.

Evans AL, Brice G, Sotirova V, Mortimer P, Beninson J, Burnand K, Rosbotham J, Child A, Sarfarazi M.

Am J Hum Genet. 1999 Feb;64(2):547-55.

19.

Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.

Holberg CJ, Erickson RP, Bernas MJ, Witte MH, Fultz KE, Andrade M, Witte CL.

Am J Med Genet. 2001 Feb 1;98(4):303-12.

PMID:
11170072
20.

A linkage study of distal chromosome 5q and bipolar disorder.

Mirow AL, Kristbjanarson H, Egeland JA, Shilling P, Helgason T, Gillin JC, Hirsch S, Kelsoe JR.

Biol Psychiatry. 1994 Aug 15;36(4):223-9.

PMID:
7986886
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