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Results of search for 'au:"CONNEALLY, P M"', page 4 of 10
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Authors
Christian, J C
Conneally, P M
Edenberg, H J
Farrer, L A
Foroud, T
Goate, A
Gusella, J F
Haines, J L
Hodes, M E
Koller, D L
Lovrien, E W
Merritt, A D
Palmer, C G
Pericak-Vance, M A
Reich, T
Roses, A D
Saunders, A M
Tanzi, R E
Wexler, N S
Yu, P L
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Topics
Adolescent
Adult
Aged
Alleles
Alzheimer Disease
Chromosome Mapping
DNA
Female
Gene Frequency
Genetic Linkage
Genetic Markers
Genotype
Humans
Huntington Disease
Lod Score
Male
Middle Aged
Pedigree
Polymorphism, Genetic
genetics
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English
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61.
A test of the hypothesis that age at onset in Huntington disease is controlled by an X-linked recessive modifier.
[electronic resource]
by
Ridley, R M
Farrer, L A
Frith, C D
Conneally, P M
Producer:
19920402
In:
American journal of human genetics
vol. 50
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62.
The genetic structure of the Kuwaiti population. I. Distribution of 17 markers with genetic distance analysis.
[electronic resource]
by
Al-Nassar, K E
Conneally, P M
Palmer, C G
Yu, P
Producer:
19810723
In:
Human genetics
vol. 57
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63.
Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting.
[electronic resource]
by
Ridley, R M
Frith, C D
Farrer, L A
Conneally, P M
Producer:
19910828
In:
Journal of medical genetics
vol. 28
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64.
Anticipation in Huntington's disease is inherited through the male line but may originate in the female.
[electronic resource]
by
Ridley, R M
Frith, C D
Crow, T J
Conneally, P M
Producer:
19881219
In:
Journal of medical genetics
vol. 25
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65.
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6.
[electronic resource]
by
Eiberg, H
Bixler, D
Nielsen, L S
Conneally, P M
Mohr, J
Producer:
19871110
In:
Clinical genetics
vol. 32
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66.
Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I.
[electronic resource]
by
Merritt, A D
Lovrien, E W
Rivas, M L
Conneally, P M
Producer:
19731211
In:
American journal of human genetics
vol. 25
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67.
Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis.
[electronic resource]
by
Wallace, M R
Dwulet, F E
Conneally, P M
Benson, M D
Producer:
19860806
In:
The Journal of clinical investigation
vol. 78
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68.
Possible linear order of genes for endocrine neoplasia type 2, the P red cell antigen and HL-A on chromosome 6.
[electronic resource]
by
Jackson, C E
Conneally, P M
Sizemore, G W
Tashjian, A H
Producer:
19770125
In:
Birth defects original article series
vol. 12
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69.
Considerations in using linkage analysis as a presymptomatic test for Huntington's disease.
[electronic resource]
by
Farrer, L A
Myers, R H
Cupples, L A
Conneally, P M
Producer:
19881219
In:
Journal of medical genetics
vol. 25
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70.
Association of blood groups with essential and secondary hypertension. A possible association of the MNS system.
[electronic resource]
by
Miller, J Z
Grim, C E
Conneally, P M
Weinberger, M H
Producer:
19800616
In:
Hypertension (Dallas, Tex. : 1979)
vol. 1
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71.
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family.
[electronic resource]
by
Wallace, M R
Conneally, P M
Long, G L
Benson, M D
Producer:
19861210
In:
American journal of medical genetics
vol. 25
Online resources:
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72.
Semiautomatic digital printing caliper for tooth measurements.
[electronic resource]
by
Conneally, P M
Merritt, A D
Quinn, B E
Potter, R H
Producer:
19680802
In:
Journal of dental research
vol. 47
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73.
Huntington disease: estimation of heterozygote status using linked genetic markers.
[electronic resource]
by
Conneally, P M
Wallace, M R
Gusella, J F
Wexler, N S
Producer:
19851216
In:
Genetic epidemiology
vol. 1
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74.
The genetic structure of the Kuwaiti population II: The distribution of Q-band chromosomal heteromorphisms.
[electronic resource]
by
Al-Nassar, K E
Palmer, C G
Conneally, P M
Yu, P L
Producer:
19811215
In:
Human genetics
vol. 57
Online resources:
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75.
Age-of-onset heterogeneity in Huntington disease families.
[electronic resource]
by
Pericak-Vance, M A
Elston, R C
Conneally, P M
Dawson, D V
Producer:
19830407
In:
American journal of medical genetics
vol. 14
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76.
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.
[electronic resource]
by
Trofatter, J A
Dlouhy, S R
DeMyer, W
Conneally, P M
Hodes, M E
Producer:
19900119
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 86
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77.
Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28.
[electronic resource]
by
Kambouris, M
Dlouhy, S R
Trofatter, J A
Conneally, P M
Hodes, M E
Producer:
19880406
In:
American journal of medical genetics
vol. 29
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78.
Apolipoprotein E4 allele and Alzheimer disease: examination of allelic association and effect on age at onset in both early- and late-onset cases.
[electronic resource]
by
Locke, P A
Conneally, P M
Tanzi, R E
Gusella, J F
Haines, J L
Producer:
19950518
In:
Genetic epidemiology
vol. 12
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79.
Linkage relationships and multipoint mapping of the human parotid salivary proteins (Pr, Pa, Db).
[electronic resource]
by
Yu, P L
Karn, R C
Merritt, A D
Azen, E A
Conneally, P M
Producer:
19800926
In:
American journal of human genetics
vol. 32
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80.
Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis.
[electronic resource]
by
Wallace, M R
Dwulet, F E
Williams, E C
Conneally, P M
Benson, M D
Producer:
19880209
In:
The Journal of clinical investigation
vol. 81
Online resources:
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