Lin AE - Search Results

1

Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry.

Prakash SK, Bondy CA, Maslen CL, Silberbach M, Lin AE, Perrone L, Limongelli G, Michelena HI, Bossone E, Citro R; BAVCon Investigators, GenTAC Registry Investigators; Lemaire SA, Body SC, Milewicz DM. Prakash SK, et al. Among authors: lin ae. Am J Med Genet A. 2016 Dec;170(12):3157-3164. doi: 10.1002/ajmg.a.37953. Epub 2016 Sep 8. Am J Med Genet A. 2016. PMID: 27604636 Free PMC article.

2

Monozygotic Turner syndrome twins--correlation of phenotype severity and heart defect.

Lin AE, Garver KL. Lin AE, et al. Am J Med Genet. 1988 Mar;29(3):529-31. doi: 10.1002/ajmg.1320290309. Am J Med Genet. 1988. PMID: 3376996

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

Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND gene.

Huang T, Lin AE, Cox GF, Golden WL, Feldman GL, Ute M, Schrander-Stumpel C, Kamisago M, Vermeulen SJ. Huang T, et al. Among authors: lin ae. Genet Med. 2002 Nov-Dec;4(6):464-7. doi: 10.1097/00125817-200211000-00011. Genet Med. 2002. PMID: 12509719 Free article.

7

Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions.

Lalani SR, Stockton DW, Bacino C, Molinari LM, Glass NL, Fernbach SD, Towbin JA, Craigen WJ, Graham JM Jr, Hefner MA, Lin AE, McBride KL, Davenport SL, Belmont JW. Lalani SR, et al. Among authors: lin ae. Am J Med Genet A. 2003 Apr 30;118A(3):260-6. doi: 10.1002/ajmg.a.20002. Am J Med Genet A. 2003. PMID: 12673657

8

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.

9

Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?

Lin AE, Pober BR, Mullen MP, Slavotinek AM. Lin AE, et al. Am J Med Genet A. 2005 Dec 15;139(3):186-93. doi: 10.1002/ajmg.a.31023. Am J Med Genet A. 2005. PMID: 16283673 Review.

10

Congenital diaphragmatic hernia and associated cardiovascular malformations: type, frequency, and impact on management.

Lin AE, Pober BR, Adatia I. Lin AE, et al. Am J Med Genet C Semin Med Genet. 2007 May 15;145C(2):201-16. doi: 10.1002/ajmg.c.30131. Am J Med Genet C Semin Med Genet. 2007. PMID: 17436301 Free PMC article. Review.

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

311 results

Search Page

Filters