Milewicz DM - Search Results

1

Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders.

Milewicz DM. Milewicz DM. Tex Heart Inst J. 1994;21(1):22-9. Tex Heart Inst J. 1994. PMID: 8180508 Free PMC article. Review.

2

Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.

Putnam EA, Zhang H, Ramirez F, Milewicz DM. Putnam EA, et al. Among authors: milewicz dm. Nat Genet. 1995 Dec;11(4):456-8. doi: 10.1038/ng1295-456. Nat Genet. 1995. PMID: 7493032

3

A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndrome.

Milewicz DM, Grossfield J, Cao SN, Kielty C, Covitz W, Jewett T. Milewicz DM, et al. J Clin Invest. 1995 May;95(5):2373-8. doi: 10.1172/JCI117930. J Clin Invest. 1995. PMID: 7738200 Free PMC article.

4

Marfan syndrome. Long-term survival and complications after aortic aneurysm repair.

Finkbohner R, Johnston D, Crawford ES, Coselli J, Milewicz DM. Finkbohner R, et al. Among authors: milewicz dm. Circulation. 1995 Feb 1;91(3):728-33. doi: 10.1161/01.cir.91.3.728. Circulation. 1995. PMID: 7828300

5

Severe neonatal Marfan syndrome resulting from a de novo 3-bp insertion into the fibrillin gene on chromosome 15.

Milewicz DM, Duvic M. Milewicz DM, et al. Am J Hum Genet. 1994 Mar;54(3):447-53. Am J Hum Genet. 1994. PMID: 8116614 Free PMC article.

6

Dolichonychia in a patient with the Marfan syndrome.

Cohen PR, Milewicz DM. Cohen PR, et al. Among authors: milewicz dm. J Dermatol. 1993 Dec;20(12):779-82. doi: 10.1111/j.1346-8138.1993.tb01383.x. J Dermatol. 1993. PMID: 8120241

7

Repeat polymorphisms in human fibrillin genes on chromosome 15 (FBN1) and chromosome 5 (FBN2).

Biddinger AL, Hecht JT, Milewicz DM. Biddinger AL, et al. Among authors: milewicz dm. Hum Mol Genet. 1993 Aug;2(8):1323. doi: 10.1093/hmg/2.8.1323. Hum Mol Genet. 1993. PMID: 8401518 No abstract available.

8

Abnormal fibrillin metabolism in bovine Marfan syndrome.

Potter KA, Hoffman Y, Sakai LY, Byers PH, Besser TE, Milewicz DM. Potter KA, et al. Among authors: milewicz dm. Am J Pathol. 1993 Mar;142(3):803-10. Am J Pathol. 1993. PMID: 8456941 Free PMC article.

9

Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene.

Putnam EA, Cho M, Zinn AB, Towbin JA, Byers PH, Milewicz DM. Putnam EA, et al. Among authors: milewicz dm. Am J Med Genet. 1996 Mar 29;62(3):233-42. doi: 10.1002/(SICI)1096-8628(19960329)62:3<233::AID-AJMG7>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8882780

10

Fibrillin-1 (FBN1) mutations in patients with thoracic aortic aneurysms.

Milewicz DM, Michael K, Fisher N, Coselli JS, Markello T, Biddinger A. Milewicz DM, et al. Circulation. 1996 Dec 1;94(11):2708-11. doi: 10.1161/01.cir.94.11.2708. Circulation. 1996. PMID: 8941093

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

341 results

Search Page

Filters