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Items: 1 to 20 of 86

1.

Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7q.

Pandya A, Blanton SH, Landa B, Javaheri R, Melvin E, Nance WE, Markello T.

Genomics. 1996 Dec 1;38(2):227-30.

PMID:
8954806
2.

The hereditary pancreatitis gene maps to long arm of chromosome 7.

Le Bodic L, Bignon JD, Raguénès O, Mercier B, Georgelin T, Schnee M, Soulard F, Gagne K, Bonneville F, Muller JY, Bachner L, Férec C.

Hum Mol Genet. 1996 Apr;5(4):549-54.

PMID:
8845851
3.

A gene for hereditary pancreatitis maps to chromosome 7q35.

Whitcomb DC, Preston RA, Aston CE, Sossenheimer MJ, Barua PS, Zhang Y, Wong-Chong A, White GJ, Wood PG, Gates LK Jr, Ulrich C, Martin SP, Post JC, Ehrlich GD.

Gastroenterology. 1996 Jun;110(6):1975-80.

PMID:
8964426
4.

Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG)

Sossenheimer MJ, Aston CE, Preston RA, Gates LK Jr, Ulrich CD, Martin SP, Zhang Y, Gorry MC, Ehrlich GD, Whitcomb DC.

Am J Gastroenterol. 1997 Jul;92(7):1113-6.

PMID:
9219780
5.

Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q.

Notelet L, Chapon F, Khoury S, Vahedi K, Chodkiewicz JP, Courtheoux P, Iba-Zizen MT, Cabanis EA, Lechevalier B, Tournier-Lasserve E, Houtteville JP.

J Neurol Neurosurg Psychiatry. 1997 Jul;63(1):40-5.

6.

Linkage of the locus for cerebral cavernous hemangiomas to human chromosome 7q in four families of Mexican-American descent.

Polymeropoulos MH, Hurko O, Hsu F, Rubenstein J, Basnet S, Lane K, Dietz H, Spetzler RF, Rigamonti D.

Neurology. 1997 Mar;48(3):752-7.

PMID:
9065560
7.

Identification of a hereditary pancreatitis mutation in four West Virginia families.

Elitsur Y, Chertow BC, Jewell RD, Finver SN, Primerano DA.

Pediatr Res. 1998 Dec;44(6):927-30.

PMID:
9853929
8.

Heterogeneity in hereditary pancreatitis.

Dasouki MJ, Cogan J, Summar ML, Neblitt W 3rd, Foroud T, Koller D, Phillips JA 3rd.

Am J Med Genet. 1998 Apr 28;77(1):47-53.

PMID:
9557894
9.

Otosclerosis: a genetically heterogeneous disease involving at least three different genes.

Van Den Bogaert K, Govaerts PJ, De Leenheer EM, Schatteman I, Verstreken M, Chen W, Declau F, Cremers CW, Van De Heyning PH, Offeciers FE, Somers T, Smith RJ, Van Camp G.

Bone. 2002 Apr;30(4):624-30.

PMID:
11934656
10.

[From gene to disease; hereditary pancreatitis].

Drenth JP, Jansen JB.

Ned Tijdschr Geneeskd. 2000 Nov 25;144(48):2301-2. Review. Dutch.

PMID:
11143296
11.

Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.

Férec C, Raguénès O, Salomon R, Roche C, Bernard JP, Guillot M, Quéré I, Faure C, Mercier B, Audrézet MP, Guillausseau PJ, Dupont C, Munnich A, Bignon JD, Le Bodic L.

J Med Genet. 1999 Mar;36(3):228-32.

12.

Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.

Wolf MT, Zalewski I, Martin FC, Ruf R, Müller D, Hennies HC, Schwarz S, Panther F, Attanasio M, Acosta HG, Imm A, Lucke B, Utsch B, Otto E, Nurnberg P, Nieto VG, Hildebrandt F.

Nephrol Dial Transplant. 2005 May;20(5):909-14. Epub 2005 Mar 1.

PMID:
15741201
13.

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.

Greinwald JH Jr, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ.

Am J Med Genet. 1998 Jun 30;78(2):107-13.

PMID:
9674898
14.

Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.

Kenna P, Mansergh F, Millington-Ward S, Erven A, Kumar-Singh R, Brennan R, Farrar GJ, Humphries P.

Br J Ophthalmol. 1997 Mar;81(3):207-13.

15.

An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12.

Yamada K, Tomita H, Yoshiura K, Kondo S, Wakui K, Fukushima Y, Ikegawa S, Nakamura Y, Amemiya T, Niikawa N.

Eur J Hum Genet. 2000 Jul;8(7):535-9.

16.

A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.

Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y.

Mol Vis. 2007 Aug 1;13:1357-62.

PMID:
17768382
17.

Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31.

Evans JC, Frayling TM, Ellard S, Gutowski NJ.

Hum Genet. 2000 Jun;106(6):636-8.

PMID:
10942112
18.

Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18.

Tetens J, Ganter M, Müller G, Drögemüller C.

Invest Ophthalmol Vis Sci. 2007 Aug;48(8):3506-15.

PMID:
17652717
19.

Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3.

Nakagawa H, Koyama K, Tanaka T, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Monden M, Nakamura Y.

Hum Genet. 1998 Feb;102(2):203-6.

PMID:
9521590
20.

An autosomal dominant progressive congenital zonular nuclear cataract linked to chromosome 20p12.2-p11.23.

Li N, Yang Y, Bu J, Zhao C, Lu S, Zhao J, Yan L, Cui L, Zheng R, Li J, Tang J, Zhao K.

Mol Vis. 2006 Dec 5;12:1506-10.

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