Lin AE - Search Results

1

Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management.

Lin AE, Basson CT, Goldmuntz E, Magoulas PL, McDermott DA, McDonald-McGinn DM, McPherson E, Morris CA, Noonan J, Nowak C, Pierpont ME, Pyeritz RE, Rope AF, Zackai E, Pober BR. Lin AE, et al. Genet Med. 2008 Jul;10(7):469-94. doi: 10.1097/gim.0b013e3181772111. Genet Med. 2008. PMID: 18580689 Free PMC article. Review.

2

Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.

Lin AE, Garver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J. Lin AE, et al. Am J Med Genet. 1988 Nov;31(3):533-48. doi: 10.1002/ajmg.1320310308. Am J Med Genet. 1988. PMID: 3067575 Review.

3

Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.

Ramer JC, Lin AE, Dobyns WB, Winter R, Aymé S, Pallotta R, Ladda RL. Ramer JC, et al. Among authors: lin ae. Am J Med Genet. 1995 Jul 3;57(3):403-9. doi: 10.1002/ajmg.1320570308. Am J Med Genet. 1995. PMID: 7545868 Review.

4

Further delineation of the branchio-oculo-facial syndrome.

Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P, et al. Lin AE, et al. Am J Med Genet. 1995 Mar 13;56(1):42-59. doi: 10.1002/ajmg.1320560112. Am J Med Genet. 1995. PMID: 7747785 Free article. Review.

5

Further delineation of the Baller-Gerold syndrome.

Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ. Lin AE, et al. Am J Med Genet. 1993 Feb 15;45(4):519-24. doi: 10.1002/ajmg.1320450423. Am J Med Genet. 1993. PMID: 8465861 Review.

6

Cardiac anomalies in the Simpson-Golabi-Behmel syndrome.

Lin AE, Neri G, Hughes-Benzie R, Weksberg R. Lin AE, et al. Am J Med Genet. 1999 Apr 23;83(5):378-81. Am J Med Genet. 1999. PMID: 10232747 Review.

7

Cardiovascular malformations: changes in prevalence and birth status, 1972-1990.

Lin AE, Herring AH, Amstutz KS, Westgate MN, Lacro RV, Al-Jufan M, Ryan L, Holmes LB. Lin AE, et al. Am J Med Genet. 1999 May 21;84(2):102-10. Am J Med Genet. 1999. PMID: 10323733

8

Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome.

Lin AE, Semina EV, Daack-Hirsch S, Roeder ER, Curry CJ, Rosenbaum K, Weaver DD, Murray JC. Lin AE, et al. Am J Med Genet. 2000 Apr 24;91(5):387-90. doi: 10.1002/(sici)1096-8628(20000424)91:5<387::aid-ajmg13>3.0.co;2-1. Am J Med Genet. 2000. PMID: 10767004

9

Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1.

Lin AE, Birch PH, Korf BR, Tenconi R, Niimura M, Poyhonen M, Armfield Uhas K, Sigorini M, Virdis R, Romano C, Bonioli E, Wolkenstein P, Pivnick EK, Lawrence M, Friedman JM. Lin AE, et al. Am J Med Genet. 2000 Nov 13;95(2):108-17. doi: 10.1002/1096-8628(20001113)95:2<108::aid-ajmg4>3.0.co;2-0. Am J Med Genet. 2000. PMID: 11078559

10

Heterotaxy: associated conditions and hospital-based prevalence in newborns.

Lin AE, Ticho BS, Houde K, Westgate MN, Holmes LB. Lin AE, et al. Genet Med. 2000 May-Jun;2(3):157-72. doi: 10.1097/00125817-200005000-00002. Genet Med. 2000. PMID: 11256661 Free article.

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