GATA4 sequence variants in patients with congenital heart disease von Tomita-Mitchell, A, Maslen, C L, Morris, C D, Garg, V, Goldmuntz, E

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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene von DIETZ, H. C, CUTTING, G. R, STETTEN, G, MEYERS, D. A, FRANCOMANO, C. A, PYERITZ, R. E, MASLEN, C. L, SAKAI, L. Y, CORSON, G. M, PUFFENBERGER, E. G, HAMOSH, A, NANTHAKUMAR, E. J, CURRISTIN, S. M

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Partial sequence of a candidate gene for the Marfan syndrome von MASLEN, C. L, CORSON, G. M, MADDOX, B. K, GLANVILLE, R. W, SAKAI, L. Y

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Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene von DIETZ, H. C, PYERITZ, R. E, PUFFENBERGER, E. G, KENDZIOR, R. J, CORSON, G. M, MASLEN, C. L, SAKAI, L. Y, FRANCOMANO, C. A, CUTTING, G. R

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PTPN11 mutations play a minor role in isolated congenital heart disease von Weismann, Constance G., Hager, A., Kaemmerer, H., Maslen, C. L., Morris, Cynthia D., Schranz, D., Kreuder, J., Gelb, B.D.

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Type VI Collagen Anchors Endothelial Basement Membranes by Interacting with Type IV Collagen von Kuo, Huey-Ju, Maslen, Cheryl L., Keene, Douglas R., Glanville, Robert W.

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Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1 von Magenis, R.Ellen, Maslen, Cheryl L., Smith, Leslie, Allen, Leland, Sakai, Lynn Y.

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Calcium binding, hydroxylation, and glycosylation of the precursor epidermal growth factor-like domains of fibrillin-1, the Marfan gene protein von Glanville, R W, Qian, R Q, McClure, D W, Maslen, C L

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Occurrence of a mutation associated with Wolman disease in a family with cholesteryl ester storage disease von Maslen, C. L., Babcock, D., Illingworth, D. R.

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Angiotensin-converting enzyme DD genotype and cardiovascular disease in heterozygous familial hypercholesterolemia von O'Malley, J P, Maslen, C L, Illingworth, D R

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A BamHI polymorphism at the fibrillin (FBN) locus von CLARK, B. A, MASLEN, C. L, SAKAI, L. Y, AL DHALIMI, A, LITT, R, LITT, M

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Missense Mutations in CRELD1 Are Associated with Cardiac Atrioventricular Septal Defects von Robinson, Susan W., Morris, Cynthia D., Goldmuntz, Elizabeth, Reller, Mark D., Jones, Melanie A., Steiner, Robert D., Maslen, Cheryl L.

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Role of the community pharmacist in the care of patients with chronic schizophrenia in the community von MASLEN, C. L., REES, L., REDFERN, P. H.

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Angiotensin-converting enzyme and cardiovascular disease risk von O'Malley, J P, Maslen, C L, Illingworth, D R

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Molecular genetics of atrioventricular septal defects von Maslen, Cheryl L

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Carrier Frequency of the Common Mutation IVS8-1G>C in DHCR7 and Estimate of the Expected Incidence of Smith–Lemli–Opitz Syndrome von Battaile, Kevin P., Battaile, Brian C., Merkens, Louise S., Maslen, Cheryl L., Steiner, Robert D.

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The molecular basis of Marfan syndrome von Maslen, C L, Glanville, R W

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Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins von Rupp, Paul A, Fouad, Gameil T, Egelston, Carley A, Reifsteck, Carol A, Olson, Susan B, Knosp, Wendy M, Glanville, Robert W, Thornburg, Kent L, Robinson, Susan W, Maslen, Cheryl L

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CRELD2: Gene mapping, alternate splicing, and comparative genomic identification of the promoter region von Maslen, Cheryl L., Babcock, Darcie, Redig, Jennifer K., Kapeli, Katannya, Akkari, Yassmine M., Olson, Susan B.

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Smith-Lemli-Opitz Syndrome: A Multiple Malformation/Mental Retardation Syndrome Caused By Defective Cholesterol Synthesis von Ginat, Sharon, Maslen, Cheryl L., Connor, William E., Porter, Forbes D., Steiner, Robert D.

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