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TY  - JOUR
AU  - Beuren, A.J.
TI  - Supravalvular aortic stenosis: a complex syndrome with and without mental retardation
JO  - Birth Defects
PY  - 1972///
VL  - 8
SP  - 45
EP  - 46
ER  - 

TY  - JOUR
AU  - Morris, C.A.
AU  - Demsey, S.A.
AU  - Leonard, C.O.
AU  - Dilts, C.
AU  - Blackburn, B.L.
TI  - Natural history of Williams syndrome
JO  - J. Pediatr.
PY  - 1988///
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EP  - 326
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TY  - JOUR
AU  - Bellugi, U.
AU  - Bihrle, A.
AU  - Jernigan, T.
AU  - Trauner, D.
AU  - Doherty, S.
TI  - rophysical, neurological, and neuroanatomical profile of Williams syndrome
JO  - Am. J. med. Genet.
PY  - 1990///
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SP  - 115
EP  - 125
ER  - 

TY  - JOUR
AU  - Dilts, C.
AU  - Morris, C.
AU  - Leonard, C.
TI  - Hypothesis for development of a behavioral phenotype in Williams syndrome
JO  - Am. J. med. Genet.
PY  - 1990///
VL  - 6
SP  - 126
EP  - 131
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TY  - JOUR
AU  - Chevers, N.
TI  - Observations on the diseases of the orifice and valves of the aorta
JO  - Hosp. Rep.
PY  - 1842///
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TY  - JOUR
AU  - Eisenberg, R.
AU  - Young, D.
AU  - Jacobson, B.
AU  - Voito, A.
TI  - Familial supravalvular aortic stenosis
JO  - Am J. Dis. Child.
PY  - 1964///
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SP  - 347
EP  - 347
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TY  - JOUR
AU  - Ewart, A.K.
TI  - A human vascular disorder, supravalvuar aortic stenosis, maps to chromosome 7
JO  - Proc. natn. Acad. Sci. U.S.A.
PY  - 1993///
VL  - 90
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TY  - JOUR
AU  - Curran, M.E.
TI  - The eiastin gene is disrupted by a translocation associated with supravalvular aortic stenosis
JO  - Cell
PY  - 1993///
VL  - 73
SP  - 159
EP  - 168
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UR  - http://dx.doi.org/10.1016/0092-8674(93)90168-P
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TY  - JOUR
AU  - Morris, C.
AU  - Thomas, I.T.
AU  - Greenberg, F.
TI  - Williams syndrome: autosomal dominant inheritance
JO  - Am. J. med. Genet.
PY  - ///
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TY  - JOUR
AU  - Tromp, G.
TI  - A to G polymorphism in ELN gene
JO  - Nucl. Acids Res.
PY  - 1991///
VL  - 19
SP  - 4314
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TY  - JOUR
AU  - Perou, M.
TI  - Congenital supravalvular aortic stenosis
JO  - Arch. Pathol.
PY  - 1961///
VL  - 71
SP  - 113
EP  - 126
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TY  - JOUR
AU  - O'Connor, W.
TI  - Supravalvular aortic stenosis: clinical and pathologic observations in six patients
JO  - Arch. Pathol. Lab. Med.
PY  - 1985///
VL  - 109
SP  - 179
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TY  - JOUR
AU  - Morris, C.A.
AU  - Loker, J.
AU  - Ensing, G.
AU  - Stock, A.D.
TI  - Supravalvular aortic stenosis cosegregates with a familial 6;7 translocation which disrupts the elastin gene
JO  - Am. J. med. Genet.
PY  - 1993///
VL  - 46
SP  - 737
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TY  - JOUR
AU  - Wahl, G.M.
TI  - Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer
JO  - Proc. natn. Acad. Sci. U.S.A.
PY  - 1987///
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TY  - JOUR
AU  - Benton, W.D.
AU  - Davis, R.W.
TI  - Screening I-gt recombinant clones by hybridization to single plaques in situ
JO  - Science
PY  - 1977///
VL  - 196
SP  - 180
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AU  - Southern, E.M.
TI  - Detection of specific sequences among DNA fragments separated by gel electrophoresis
JO  - J. molec. Biol.
PY  - 1975///
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AU  - Curran, M.E.
AU  - Landes, G.M.
AU  - Keating, M.T.
TI  - Molecular cloning, characterization and genomic organization of a human cardiac potassium channel gene
JO  - Genomics
PY  - 1992///
VL  - 12
SP  - 729
EP  - 737
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TY  - JOUR
AU  - Kunkel, L.M.
TI  - Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants
JO  - Proc. natn. Acad. Sci. U.S.A
PY  - 1977///
VL  - 74
SP  - 1245
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TY  - JOUR
AU  - Goodman, B.K.
AU  - Xu, W.
AU  - Nottoli, V.
AU  - Rundall-Jackson, T.
AU  - Stock, A.D.
TI  - A simple technique for bone marrow preparations with modified hypotonic treatment
JO  - Karyogram
PY  - 1985///
VL  - 11
SP  - 95
EP  - 96
ER  - 

TY  - JOUR
AU  - Klever, M.
AU  - Grond-Ginsbach, C.
AU  - Scherthan, H.
AU  - Schroeder-Kurth, T.M.
TI  - Chromosomal in situ hybridization after giemsa banding
JO  - Hum. Genet.
PY  - 1991///
VL  - 86
SP  - 484
EP  - 486
ER  - 

TY  - JOUR
AU  - Pinkel, D.
TI  - Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4
JO  - Proc. natn. Acad. Sci. U.S.A.
PY  - 1988///
VL  - 85
SP  - 9138
EP  - 9142
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TY  - JOUR
AU  - Tkachuk, D.
TI  - Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridization
JO  - Science
PY  - 1990///
VL  - 250
SP  - 559
EP  - 562
ER  - 

TY  - JOUR
AU  - Fazio, M.J.
TI  - Human elastin gene: new evidence for localization of elastin to the long arm of chromosome 7
JO  - Am. J. hum. Genet.
PY  - 1991///
VL  - 48
SP  - 696
EP  - 703
ER  - 

TY  - JOUR
AU  - O'Connell, P.
TI  - Twenty loci form a continuous linkage map of marker for human chromosome 2
JO  - Genomics
PY  - 1989///
VL  - 5
SP  - 738
EP  - 745
ER  - 

TY  - JOUR
AU  - Vogelstein, B.
TI  - Allelotype of colorectal carcinomas
JO  - Science
PY  - 1989///
VL  - 244
SP  - 207
EP  - 211
ER  - 

TY  - JOUR
AU  - Nakamura, Y.
TI  - Variable number of tandem repeat markers for human gene mapping
JO  - Science
PY  - 1987///
VL  - 235
SP  - 1616
EP  - 1622
ER  - 

TY  - JOUR
AU  - Nakamura, Y.
TI  - A mapped set of DNA markers for human chromosome 17
JO  - Genomics
PY  - 1988///
VL  - 2
SP  - 302
EP  - 309
ER  - 

TY  - JOUR
AU  - Preus, M.
TI  - Williams syndrome: Objective definition and diagnosis
JO  - Clin. Genet.
PY  - 1984///
VL  - 24
SP  - 433
EP  - 438
ER  - 

