Conneally PM - Search Results

1

Possible linear order of genes for endocrine neoplasia type 2, the P red cell antigen and HL-A on chromosome 6.

Jackson CE, Conneally PM, Sizemore GW, Tashjian AH. Jackson CE, et al. Among authors: conneally pm. Birth Defects Orig Artic Ser. 1976;12(1):159-64. Birth Defects Orig Artic Ser. 1976. PMID: 990440 No abstract available.

2

Linkage relations of the loci for Kell and phenylthiocarbamide taste sensitivity.

Conneally PM, Dumont-Driscoll M, Huntzinger RS, Nance WE, Jackson CE. Conneally PM, et al. Hum Hered. 1976;26(4):267-71. doi: 10.1159/000152813. Hum Hered. 1976. PMID: 976995

3

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.

Young K, Foroud T, Williams P, Jackson CE, Beckmann JS, Cohen D, Conneally PM, Tischfield J, Hodes ME. Young K, et al. Among authors: conneally pm. Genomics. 1992 Aug;13(4):1370-1. doi: 10.1016/0888-7543(92)90074-3. Genomics. 1992. PMID: 1505977 No abstract available.

4

Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15.

Velinov M, Sarfarazi M, Young K, Hodes ME, Conneally PM, Jackson CE, Tsipouras P. Velinov M, et al. Among authors: conneally pm. Connect Tissue Res. 1993;29(1):13-21. doi: 10.3109/03008209309061962. Connect Tissue Res. 1993. PMID: 8339542

5

Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus.

Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS. Allamand V, et al. Among authors: conneally pm. Hum Mol Genet. 1995 Mar;4(3):459-63. doi: 10.1093/hmg/4.3.459. Hum Mol Genet. 1995. PMID: 7795603

6

Linkage relations of the loci for the MN blood group and red cell acid phosphatase.

Weitkamp LR, Lovrien EW, Olaisen B, Fenger K, Gedde-Dahl T Jr, Sorensen SA, Conneally PM, Bias WB, Ott J. Weitkamp LR, et al. Among authors: conneally pm. Birth Defects Orig Artic Ser. 1975;11(3):276-80. Birth Defects Orig Artic Ser. 1975. PMID: 1203495 No abstract available.

7

Linkage group I: multipoint mapping.

Meyers DA, Conneally PM, Hecht F, Lovrien EW, Magenis E, Merritt AD, Palmer CG, Rivas ML, Wang L. Meyers DA, et al. Among authors: conneally pm. Birth Defects Orig Artic Ser. 1975;11(3):211-9. Birth Defects Orig Artic Ser. 1975. PMID: 812567 No abstract available.

8

Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh.

Rivas ML, Conneally PM, Hecht F, Lovrien EW, Magenis E, Merritt AD, Meyers DA, Palmer CG, Wang L. Rivas ML, et al. Among authors: conneally pm. Birth Defects Orig Artic Ser. 1975;11(3):239-47. Birth Defects Orig Artic Ser. 1975. PMID: 812569 No abstract available.

9

The linkage and mapping relationships of 1qh.

Rivas ML, Conneally PM, Lovrien EW, Magenis RE, Merritt AD, Meyers DA, Palmer CG, Parks M, Wang L, Yu PL. Rivas ML, et al. Among authors: conneally pm. Birth Defects Orig Artic Ser. 1976;12(7):347-50. Birth Defects Orig Artic Ser. 1976. PMID: 1024639 No abstract available.

10

Linkage group I: the simultaneous estimation of recombination and interference.

Meyers DA, Conneally PM, Lovrien EW, Magenis RE, Merritt AD, Norton JA, Palmer CG, Rivas ML, Wang L, Yu PL. Meyers DA, et al. Among authors: conneally pm. Birth Defects Orig Artic Ser. 1976;12(7):335-9. Birth Defects Orig Artic Ser. 1976. PMID: 1024636 No abstract available.

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