Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 112

Similar articles for PubMed (Select 8964426)

1.

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
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.

3.

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
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.

Implications of molecular diagnostic testing in families with hereditary pancreatitis.

Pandya A, Xia XJ, Blanton SH, Landa B, Markello T, Nance WE.

Genet Test. 1997-1998;1(3):207-11.

PMID:
10464647
6.

Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.

Malik S, Grzeschik KH.

Hum Genet. 2008 Mar;123(2):197-205. doi: 10.1007/s00439-007-0458-4. Epub 2008 Jan 10.

PMID:
18193458
7.

Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?

Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.

Neurology. 2008 Feb 26;70(9):686-94. Epub 2007 Nov 21.

PMID:
18032746
8.

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.

9.

Autosomal dominant gnathodiaphyseal dysplasia maps to chromosome 11p14.3-15.1.

Tsutsumi S, Kamata N, Maruoka Y, Ando M, Tezuka O, Enomoto S, Omura K, Nagayama M, Kudo E, Moritani M, Yamaoka T, Itakura M.

J Bone Miner Res. 2003 Mar;18(3):413-8.

PMID:
12619924
10.

New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.

Paluru P, Ronan SM, Heon E, Devoto M, Wildenberg SC, Scavello G, Holleschau A, Mäkitie O, Cole WG, King RA, Young TL.

Invest Ophthalmol Vis Sci. 2003 May;44(5):1830-6.

PMID:
12714612
11.

Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21.

Volders PG, Zhu Q, Timmermans C, Eurlings PM, Su X, Arens YH, Li L, Jongbloed RJ, Xia M, Rodriguez LM, Chen YH.

Heart Rhythm. 2007 Apr;4(4):469-75. Epub 2006 Dec 15.

PMID:
17399636
12.

A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter.

Higgins JJ, Rosen DR, Loveless JM, Clyman JC, Grau MJ.

Neurology. 2000 Aug 8;55(3):335-40.

PMID:
10932263
13.

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.

Preston RA, Post JC, Keats BJ, Aston CE, Ferrell RE, Priest J, Nouri N, Losken HW, Morris CA, Hurtt MR, et al.

Nat Genet. 1994 Jun;7(2):149-53.

PMID:
7920632
14.

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.

Brkanac Z, Bylenok L, Fernandez M, Matsushita M, Lipe H, Wolff J, Nochlin D, Raskind WH, Bird TD.

Arch Neurol. 2002 Aug;59(8):1291-5. Erratum in: Arch Neurol 2002 Dec;59(12):1972.

PMID:
12164726
15.

Gene for progressive familial heart block type I maps to chromosome 19q13.

Brink PA, Ferreira A, Moolman JC, Weymar HW, van der Merwe PL, Corfield VA.

Circulation. 1995 Mar 15;91(6):1633-40.

16.

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
17.

A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.

Klein C, Schilling K, Saunders-Pullman RJ, Garrels J, Breakefield XO, Brin MF, deLeon D, Doheny D, Fahn S, Fink JS, Forsgren L, Friedman J, Frucht S, Harris J, Holmgren G, Kis B, Kurlan R, Kyllerman M, Lang AE, Leung J, Raymond D, Robishaw JD, Sanner G, Schwinger E, Tabamo RE, Tagliati M.

Am J Hum Genet. 2000 Nov;67(5):1314-9. Epub 2000 Oct 5.

18.

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

Weiler T, Greenberg CR, Zelinski T, Nylen E, Coghlan G, Crumley MJ, Fujiwara TM, Morgan K, Wrogemann K.

Am J Hum Genet. 1998 Jul;63(1):140-7.

19.

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.

20.

Identification of a novel locus on 2q for autosomal dominant high-grade myopia.

Paluru PC, Nallasamy S, Devoto M, Rappaport EF, Young TL.

Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2300-7.

PMID:
15980214
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk