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Results of search for 'au:"LOVRIEN, E"', page 3 of 4
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Authors
Beals, R K
Bigley, R H
Chamberlin, J
Conneally, P M
DuVal, M C
Hecht, F
Koler, R D
Linder, D
Litt, M
Lovrien, E
Lovrien, E W
Magenis, E
Magenis, R E
Merritt, A D
Meyers, D A
Ott, J
Overton, K M
Palmer, C G
Rivas, M L
Wang, L
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Adolescent
Adult
Blood Group Antigens
Child
Child, Preschool
Chromosome Aberrations
Chromosome Mapping
Chromosomes, Human, 1-3
Female
Genetic Linkage
Humans
Infant
Infant, Newborn
Karyotyping
Male
Pedigree
Recombination, Genetic
analysis
enzymology
genetics
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41.
CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series.
[electronic resource]
by
Chen, S H
Zhang, M
Lovrien, E W
Scott, C R
Thompson, A R
Producer:
19910813
In:
Human genetics
vol. 87
Online resources:
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42.
Human centromere mapping using teratoma data.
[electronic resource]
by
Ott, J
Hecht, F
Linder, D
Lovrien, E W
Kaiser, B
McCaw, B K
Producer:
19761223
In:
Cytogenetics and cell genetics
vol. 16
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43.
The 8p- syndrome.
[electronic resource]
by
Reiss, J A
Brenes, P M
Chamberlin, J
Magenis, R E
Lovrien, E W
Producer:
19790725
In:
Human genetics
vol. 47
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44.
Linkage analysis in lattice corneal dystrophy.
[electronic resource]
by
Kivlin, J D
Lovrien, E W
Maumenee, I H
Bishop, D T
Bias, W
Producer:
19841228
In:
American journal of medical genetics
vol. 19
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45.
SYMPOSIUM: BATTERED CHILD SYNDROME.
[electronic resource]
by
SULLIVAN, E
SMITH, D F
FOX, M A
LOPRESTI, J M
LOVRIEN, E
NEWSOME, M E
Producer:
19961201
In:
Clinical proceedings - Children's Hospital of the District of Columbia
vol. 20
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46.
Linkage study of antithrombin III.
[electronic resource]
by
Lovrien, E W
Magenis, R E
Rivas, M L
Goodnight, S
Moreland, R
Rowe, S
Producer:
19790925
In:
Cytogenetics and cell genetics
vol. 22
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47.
Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts.
[electronic resource]
by
Bodker, F S
Lavery, M A
Mitchell, T N
Lovrien, E W
Maumenee, I H
Producer:
19901205
In:
American journal of medical genetics
vol. 37
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48.
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
[electronic resource]
by
Litt, M
Kramer, P
LaMorticella, D M
Murphey, W
Lovrien, E W
Weleber, R G
Producer:
19980416
In:
Human molecular genetics
vol. 7
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49.
Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations.
[electronic resource]
by
Hecht, F
Case, M P
Lovrien, E W
Higgins, J V
Thuline, H C
Melnyk, J
Producer:
19680829
In:
Science (New York, N.Y.)
vol. 161
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50.
Structural and functional basis of the developmental regulation of human coagulation factor IX gene: factor IX Leyden.
[electronic resource]
by
Hirosawa, S
Fahner, J B
Salier, J P
Wu, C T
Lovrien, E W
Kurachi, K
Producer:
19900719
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 87
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51.
Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
[electronic resource]
by
Magenis, R E
Koler, R D
Lovrien, E
Bigley, R H
DuVal, M C
Overton, K M
Producer:
19770611
In:
Birth defects original article series
vol. 12
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52.
Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2.
[electronic resource]
by
Magenis, R E
Koler, R D
Lovrien, E
Bigley, R H
DuVal, M C
Overton, K M
Producer:
19760219
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 72
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53.
Resolution of breakpoints in a complex rearrangement by use of multiple staining techniques: confirmation of suspected 12p12.3 intraband by deletion dosage effect of LDHB.
[electronic resource]
by
Magenis, E
Brown, M G
Chamberlin, J
Donlon, T
Hepburn, D
Lamvik, N
Lovrien, E
Yoshitomi, M
Producer:
19810925
In:
American journal of medical genetics
vol. 9
Online resources:
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54.
Ovarian teratomas: cytologic data.
[electronic resource]
by
McCaw, B
Hecht, F
Linder, D
Lovrien, E W
Wyandt, H
Bacon, D
Clark, B
Lea, N
Producer:
19770611
In:
Birth defects original article series
vol. 12
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55.
Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
[electronic resource]
by
Magenis, R E
Koler, R D
Lovrien, E
Bigley, R H
DuVal, M C
Overton, K M
Producer:
19761223
In:
Cytogenetics and cell genetics
vol. 16
Online resources:
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56.
Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16.
[electronic resource]
by
Lovrien, E W
Magenis, R E
Rivas, M L
Lamvik, N
Rowe, S
Wood, J
Hemmerling, J
Producer:
19790925
In:
Cytogenetics and cell genetics
vol. 22
Online resources:
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57.
A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.
[electronic resource]
by
Kramer, P
Yount, J
Mitchell, T
LaMorticella, D
Carrero-Valenzuela, R
Lovrien, E
Maumenee, I
Litt, M
Producer:
19961220
In:
Genomics
vol. 35
Online resources:
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58.
Tandem duplication of proximal 22q: a cause of cat-eye syndrome.
[electronic resource]
by
Reiss, J A
Weleber, R G
Brown, M G
Bangs, C D
Lovrien, E W
Magenis, R E
Producer:
19850308
In:
American journal of medical genetics
vol. 20
Online resources:
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59.
Ovarian teratomas: cytologic data.
[electronic resource]
by
McCaw, B K
Hecht, F
Linder, D
Lovrien, E W
Wyandt, H
Bacon, D
Clark, B
Lea, N
Producer:
19761223
In:
Cytogenetics and cell genetics
vol. 16
Online resources:
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60.
Hemoglobin Casper: beta 106 (G8) Leu leads to Pro; a contemporary mutation.
[electronic resource]
by
Koler, R D
Jones, R T
Bigley, R H
Litt, M
Lovrien, E
Brooks, R
Lahey, M E
Fowler, R
Producer:
19731213
In:
The American journal of medicine
vol. 55
Online resources:
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