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Results of search for 'au:"Milewicz, D M"', page 1 of 3
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Authors
Adès, L C
Arnett, F C
Bamshad, M
Basson, C T
Bateman, J F
Biddinger, A
Byers, P H
Cao, S N
Chakraborty, R
Chen, H
Child, A
Coselli, J
Coselli, J S
Crawford, E S
Guo, D
Haan, E A
Milewicz, D M
Park, E S
Putnam, E A
Tan, F K
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Topics
Adolescent
Adult
Animals
Aortic Aneurysm, Thoracic
Aortic Dissection
Base Sequence
Child
Female
Fibrillin-1
Fibrillins
Fibroblasts
Humans
Male
Marfan Syndrome
Microfilament Proteins
Molecular Sequence Data
Mutation
Pedigree
genetics
metabolism
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English
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1.
Ultrasonic characterization of the aortic architecture in Marfan patients.
[electronic resource]
by
Milewicz, D M
Producer:
19950315
In:
Circulation
vol. 91
Online resources:
Available from publisher's website
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2.
Molecular genetics of Marfan syndrome and Ehlers-Danlos type IV.
[electronic resource]
by
Milewicz, D M
Producer:
19980928
In:
Current opinion in cardiology
vol. 13
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3.
Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders.
[electronic resource]
by
Milewicz, D M
Producer:
19940615
In:
Texas Heart Institute journal
vol. 21
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4.
Severe neonatal Marfan syndrome resulting from a de novo 3-bp insertion into the fibrillin gene on chromosome 15.
[electronic resource]
by
Milewicz, D M
Duvic, M
Producer:
19940325
In:
American journal of human genetics
vol. 54
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5.
Genetics of cardiovascular disease.
[electronic resource]
by
Milewicz, D M
Seidman, C E
Producer:
20001214
In:
Circulation
vol. 102
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6.
Dolichonychia in a patient with the Marfan syndrome.
[electronic resource]
by
Cohen, P R
Milewicz, D M
Producer:
19940407
In:
The Journal of dermatology
vol. 20
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7.
Genetic disorders of the elastic fiber system.
[electronic resource]
by
Milewicz, D M
Urbán, Z
Boyd, C
Producer:
20010215
In:
Matrix biology : journal of the International Society for Matrix Biology
vol. 19
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8.
The potential role of the elastic fiber system in adolescent idiopathic scoliosis.
[electronic resource]
by
Hadley-Miller, N
Mims, B
Milewicz, D M
Producer:
19940913
In:
The Journal of bone and joint surgery. American volume
vol. 76
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9.
Familial thoracic aortic aneurysms and dissections.
[electronic resource]
by
Prahlow, J A
Barnard, J J
Milewicz, D M
Producer:
19981230
In:
Journal of forensic sciences
vol. 43
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10.
Familial thoracic aortic dilatations and dissections: a case control study.
[electronic resource]
by
Biddinger, A
Rocklin, M
Coselli, J
Milewicz, D M
Producer:
19970416
In:
Journal of vascular surgery
vol. 25
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11.
Repeat polymorphisms in human fibrillin genes on chromosome 15 (FBN1) and chromosome 5 (FBN2).
[electronic resource]
by
Biddinger, A L
Hecht, J T
Milewicz, D M
Producer:
19931105
In:
Human molecular genetics
vol. 2
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12.
Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.
[electronic resource]
by
Putnam, E A
Zhang, H
Ramirez, F
Milewicz, D M
Producer:
19960111
In:
Nature genetics
vol. 11
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13.
Nonbacterial thrombotic endocarditis in three members of a family.
[electronic resource]
by
Leung, K L
Milewicz, D M
Phillips, M D
Barasch, E
Producer:
19970605
In:
The New England journal of medicine
vol. 336
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14.
Marfan syndrome. Long-term survival and complications after aortic aneurysm repair.
[electronic resource]
by
Finkbohner, R
Johnston, D
Crawford, E S
Coselli, J
Milewicz, D M
Producer:
19950222
In:
Circulation
vol. 91
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15.
The metacarpophalangeal profile in a family with congenital contractural arachnodactyly.
[electronic resource]
by
Guala, A
Danesino, C
Milewicz, D M
Putnam, E A
Franceschini, P
Producer:
20000512
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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16.
Marfan syndrome: defective synthesis, secretion, and extracellular matrix formation of fibrillin by cultured dermal fibroblasts.
[electronic resource]
by
Milewicz, D M
Pyeritz, R E
Crawford, E S
Byers, P H
Producer:
19920210
In:
The Journal of clinical investigation
vol. 89
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17.
A dimorphic Alu Sb-like insertion in COL3A1 is ethnic-specific.
[electronic resource]
by
Milewicz, D M
Byers, P H
Reveille, J
Hughes, A L
Duvic, M
Producer:
19961231
In:
Journal of molecular evolution
vol. 42
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18.
Processing of the fibrillin-1 carboxyl-terminal domain.
[electronic resource]
by
Ritty, T M
Broekelmann, T
Tisdale, C
Milewicz, D M
Mecham, R P
Producer:
19990429
In:
The Journal of biological chemistry
vol. 274
Online resources:
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19.
FBN1 exon 2 splicing error in a patient with Marfan syndrome.
[electronic resource]
by
Guo, D
Tan, F K
Cantu, A
Plon, S E
Milewicz, D M
Producer:
20010712
In:
American journal of medical genetics
vol. 101
Online resources:
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20.
Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human development.
[electronic resource]
by
Park, E S
Putnam, E A
Chitayat, D
Child, A
Milewicz, D M
Producer:
19981020
In:
American journal of medical genetics
vol. 78
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