Lin AE - Search Results

1

Fryns syndrome with Hirschsprung disease: support for possible neural crest involvement.

Alkuraya FS, Lin AE, Irons MB, Kimonis VE. Alkuraya FS, et al. Among authors: lin ae. Am J Med Genet A. 2005 Jan 15;132A(2):226-30. doi: 10.1002/ajmg.a.30423. Am J Med Genet A. 2005. PMID: 15580636 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

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.

4

Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literature.

Feingold M, Lin AE. Feingold M, et al. Among authors: lin ae. Am J Med Genet. 1993 Nov 15;47(7):1064-7. doi: 10.1002/ajmg.1320470726. Am J Med Genet. 1993. PMID: 8291524 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

Exclusion of growth factor gene mutations as a common cause of Sotos syndrome.

Lin AE, Liu Q, Mannheim GB, Darras BT. Lin AE, et al. Am J Med Genet. 2001 Jan 1;98(1):101-2. Am J Med Genet. 2001. PMID: 11426446

7

Further delineation of cardiac abnormalities in Costello syndrome.

Lin AE, Grossfeld PD, Hamilton RM, Smoot L, Gripp KW, Proud V, Weksberg R, Wheeler P, Picker J, Irons M, Zackai E, Marino B, Scott CI Jr, Nicholson L. Lin AE, et al. Am J Med Genet. 2002 Aug 1;111(2):115-29. doi: 10.1002/ajmg.10558. Am J Med Genet. 2002. PMID: 12210337 Review.

8

Participation by clinical geneticists in genetic advocacy groups.

Lin AE, Terry SF, Lerner B, Anderson R, Irons M. Lin AE, et al. Am J Med Genet A. 2003 May 15;119A(1):89-92. doi: 10.1002/ajmg.a.20027. Am J Med Genet A. 2003. PMID: 12707968 No abstract available.

9

Total is more than the sum of the parts: phenotyping the heart in cardiovascular genetics clinics.

Lin AE, Salbert BA, Belmont J, Smoot L. Lin AE, et al. Am J Med Genet A. 2004 Dec 1;131(2):111-4. doi: 10.1002/ajmg.a.30304. Am J Med Genet A. 2004. PMID: 15487010 No abstract available.

10

Myocardial storage of chondroitin sulfate-containing moieties in Costello syndrome patients with severe hypertrophic cardiomyopathy.

Hinek A, Teitell MA, Schoyer L, Allen W, Gripp KW, Hamilton R, Weksberg R, Klüppel M, Lin AE. Hinek A, et al. Among authors: lin ae. Am J Med Genet A. 2005 Feb 15;133A(1):1-12. doi: 10.1002/ajmg.a.30495. Am J Med Genet A. 2005. PMID: 15637729

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