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Results: 1 to 20 of 126

Similar articles for PubMed (Select 7881412)

1.

Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity.

Robin NH, Feldman GJ, Mitchell HF, Lorenz P, Wilroy RS, Zackai EH, Allanson JE, Reich EW, Pfeiffer RA, Clarke LA, et al.

Hum Mol Genet. 1994 Dec;3(12):2153-8.

PMID:
7881412
2.

Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families.

Kendler KS, MacLean CJ, O'Neill FA, Burke J, Murphy B, Duke F, Shinkwin R, Easter SM, Webb BT, Zhang J, Walsh D, Straub RE.

Am J Psychiatry. 1996 Dec;153(12):1534-40.

PMID:
8942448
3.

No evidence of linkage to 6p markers in spanish families with juvenile myoclonic epilepsy.

Obach V, Arroyo S, Santamaria J, Grinberg D, Oliva R.

Neurosci Lett. 2000 Jun 9;286(3):213-7.

PMID:
10832022
4.

Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.

Goobie S, Popovic M, Morrison J, Ellis L, Ginzberg H, Boocock GR, Ehtesham N, Bétard C, Brewer CG, Roslin NM, Hudson TJ, Morgan K, Fujiwara TM, Durie PR, Rommens JM.

Am J Hum Genet. 2001 Apr;68(4):1048-54. Epub 2001 Mar 15.

5.

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11.

Wu YQ, Heutink P, de Vries BB, Sandkuijl LA, van den Ouweland AM, Niermeijer MF, Galjaard H, Reyniers E, Willems PJ, Halley DJ.

Hum Mol Genet. 1994 Jan;3(1):167-71.

PMID:
8162019
6.

Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneity.

Génin E, Huebner A, Jaillard C, Faure A, Halaby G, Saka N, Clark AJ, Durand P, Bégeot M, Naville D.

Hum Genet. 2002 Oct;111(4-5):428-34. Epub 2002 Aug 24.

PMID:
12384787
7.

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
8.
9.

Linkage of body mass index to chromosome 20 in Utah pedigrees.

Hunt SC, Abkevich V, Hensel CH, Gutin A, Neff CD, Russell DL, Tran T, Hong X, Jammulapati S, Riley R, Weaver-Feldhaus J, Macalma T, Richards MM, Gress R, Francis M, Thomas A, Frech GC, Adams TD, Shattuck D, Stone S.

Hum Genet. 2001 Sep;109(3):279-85.

PMID:
11702208
10.
11.

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
12.

Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.

Collier DA, Barrett TG, Curtis D, Macleod A, Arranz MJ, Maassen JA, Bundey S.

Am J Hum Genet. 1996 Oct;59(4):855-63.

13.

Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental Glomerulosclerosis.

Winn MP, Conlon PJ, Lynn KL, Howell DN, Gross DA, Rogala AR, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance JM.

Kidney Int. 1999 Apr;55(4):1241-6.

14.

The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q.

Kibar Z, Der Kaloustian VM, Brais B, Hani V, Fraser FC, Rouleau GA.

Hum Mol Genet. 1996 Apr;5(4):543-7.

15.

Possible genetic heterogeneity in the Saethre-Chotzen syndrome.

Ma HW, Lajeunie E, de Parseval N, Munnich A, Renier D, Le Merrer M.

Hum Genet. 1996 Aug;98(2):228-32.

PMID:
8698349
16.

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.

Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.

Mov Disord. 2006 Jan;21(1):28-33.

PMID:
16124010
17.

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T.

Hum Mol Genet. 1994 Aug;3(8):1263-7.

PMID:
7987300
18.

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.

Finck A, Van der Meer JW, Schäffer AA, Pfannstiel J, Fieschi C, Plebani A, Webster AD, Hammarström L, Grimbacher B.

Eur J Hum Genet. 2006 Jul;14(7):867-75. Epub 2006 Apr 26.

19.

Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity.

Oldridge M, Temple IK, Santos HG, Gibbons RJ, Mustafa Z, Chapman KE, Loughlin J, Wilkie AO.

Am J Hum Genet. 1999 Feb;64(2):578-85.

20.

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
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