Lin AE - Search Results

1

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.

2

The branchio-oculo-facial syndrome.

Lin AE, Losken HW, Jaffe R, Biglan AW. Lin AE, et al. Cleft Palate Craniofac J. 1991 Jan;28(1):96-102. doi: 10.1597/1545-1569_1991_028_0096_tbofs_2.3.co_2. Cleft Palate Craniofac J. 1991. PMID: 2004100 Review.

3

Central nervous system malformations in the CHARGE association.

Lin AE, Siebert JR, Graham JM Jr. Lin AE, et al. Am J Med Genet. 1990 Nov;37(3):304-10. doi: 10.1002/ajmg.1320370303. Am J Med Genet. 1990. PMID: 2260555 Review.

4

Craniosynostosis, agenesis of the corpus callosum, serve mental retardation, distinctive facies, camptodactyly, and hypogonadism.

Lin AE, Gettig E. Lin AE, et al. Am J Med Genet. 1990 Apr;35(4):582-5. doi: 10.1002/ajmg.1320350427. Am J Med Genet. 1990. PMID: 2333890 No abstract available.

5

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.

6

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

7

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.

8

Maldescent of the thymus.

Lin AE, Gorlin RJ. Lin AE, et al. Pediatr Pathol. 1994 Jan-Feb;14(1):177; author reply 179-80. Pediatr Pathol. 1994. PMID: 8159615 No abstract available.

9

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.

10

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.

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