Conneally PM - Search Results

1

Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28.

Kambouris M, Dlouhy SR, Trofatter JA, Conneally PM, Hodes ME. Kambouris M, et al. Among authors: conneally pm. Am J Med Genet. 1988 Jan;29(1):239-46. doi: 10.1002/ajmg.1320290138. Am J Med Genet. 1988. PMID: 2894172

2

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.

Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B. Dlouhy SR, et al. Among authors: conneally pm. Nat Genet. 1992 Apr;1(1):64-7. doi: 10.1038/ng0492-64. Nat Genet. 1992. PMID: 1363809

3

A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease.

Pratt VM, Trofatter JA, Schinzel A, Dlouhy SR, Conneally PM, Hodes ME. Pratt VM, et al. Among authors: conneally pm. Am J Med Genet. 1991 Jan;38(1):136-9. doi: 10.1002/ajmg.1320380129. Am J Med Genet. 1991. PMID: 1707231

4

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.

Dlouhy SR, Christian JC, Haines JL, Conneally PM, Hodes ME. Dlouhy SR, et al. Among authors: conneally pm. Hum Genet. 1987 Feb;75(2):136-9. doi: 10.1007/BF00591074. Hum Genet. 1987. PMID: 3469136

5

Possible localization of a major gene for cleft lip and palate to 4q.

Beiraghi S, Foroud T, Diouhy S, Bixler D, Conneally PM, Delozier-Blanchet D, Hodes ME. Beiraghi S, et al. Among authors: conneally pm. Clin Genet. 1994 Sep;46(3):255-6. doi: 10.1111/j.1399-0004.1994.tb04236.x. Clin Genet. 1994. PMID: 7820940 No abstract available.

6

Suicide risk in Huntington's disease.

Di Maio L, Squitieri F, Napolitano G, Campanella G, Trofatter JA, Conneally PM. Di Maio L, et al. Among authors: conneally pm. J Med Genet. 1993 Apr;30(4):293-5. doi: 10.1136/jmg.30.4.293. J Med Genet. 1993. PMID: 8487273 Free PMC article.

7

Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.

Trofatter JA, Dlouhy SR, DeMyer W, Conneally PM, Hodes ME. Trofatter JA, et al. Among authors: conneally pm. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9427-30. doi: 10.1073/pnas.86.23.9427. Proc Natl Acad Sci U S A. 1989. PMID: 2480601 Free PMC article.

8

Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome).

Butler MG, Hodes ME, Conneally PM, Biegel AA, Wright JC. Butler MG, et al. Among authors: conneally pm. Am J Med Genet. 1984 May;18(1):61-5. doi: 10.1002/ajmg.1320180110. Am J Med Genet. 1984. PMID: 6588752 Free PMC article.

9

Onset symptoms in 510 patients with Huntington's disease.

Di Maio L, Squitieri F, Napolitano G, Campanella G, Trofatter JA, Conneally PM. Di Maio L, et al. Among authors: conneally pm. J Med Genet. 1993 Apr;30(4):289-92. doi: 10.1136/jmg.30.4.289. J Med Genet. 1993. PMID: 8487272 Free PMC article.

10

Genetic family history questionnaire.

Cole J, Conneally PM, Hodes ME, Merritt AD. Cole J, et al. Among authors: conneally pm. J Med Genet. 1978 Feb;15(1):10-8. doi: 10.1136/jmg.15.1.10. J Med Genet. 1978. PMID: 633315 Free PMC article.

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