Lin A - Search Results

1

Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome.

Neri G, Gurrieri F, Zanni G, Lin A. Neri G, et al. Among authors: lin a. Am J Med Genet. 1998 Oct 2;79(4):279-83. doi: 10.1002/(sici)1096-8628(19981002)79:4<279::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 1998. PMID: 9781908 Review.

2

Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.

Lin AE. Lin AE. Am J Med Genet. 1993 Jun 15;46(5):606-7. doi: 10.1002/ajmg.1320460532. Am J Med Genet. 1993. PMID: 8322829 No abstract available.

3

The neuroimaging findings in Sotos syndrome.

Schaefer GB, Bodensteiner JB, Buehler BA, Lin A, Cole TR. Schaefer GB, et al. Among authors: lin a. Am J Med Genet. 1997 Feb 11;68(4):462-5. doi: 10.1002/(sici)1096-8628(19970211)68:4<462::aid-ajmg18>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9021022

4

Genetic aspects of atrioventricular septal defects.

Pierpont ME, Markwald RR, Lin AE. Pierpont ME, et al. Among authors: lin ae. Am J Med Genet. 2000 Winter;97(4):289-96. Am J Med Genet. 2000. PMID: 11376440

5

Nager acrofacial dysostosis: male-to-male transmission in 2 families.

Aylsworth AS, Lin AE, Friedman PA. Aylsworth AS, et al. Among authors: lin ae. Am J Med Genet. 1991 Oct 1;41(1):83-8. doi: 10.1002/ajmg.1320410121. Am J Med Genet. 1991. PMID: 1951468

6

Two additional patients representing the possible human homologue for the mouse mutant disorganisation (Ds).

Lin AE. Lin AE. J Med Genet. 1991 Sep;28(9):645-7. doi: 10.1136/jmg.28.9.645. J Med Genet. 1991. PMID: 1956071 Free PMC article. Review. No abstract available.

7

Noonan syndrome.

Lin AE. Lin AE. J Med Genet. 1988 Jan;25(1):64-5. doi: 10.1136/jmg.25.1.64-a. J Med Genet. 1988. PMID: 3351898 Free PMC article. No abstract available.

8

Charge association vs. velo-cardio-facial syndrome.

Lin AE. Lin AE. Am J Med Genet. 1988 Apr;29(4):951-2. doi: 10.1002/ajmg.1320290431. Am J Med Genet. 1988. PMID: 3400739 No abstract available.

9

Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.

Estop AM, Bansal V, Lin A, Levinson F, Karlin SM, Surti U, Wenger SL, Steele MW. Estop AM, et al. Among authors: lin a. Am J Med Genet. 1994 Feb 15;49(4):410-3. doi: 10.1002/ajmg.1320490412. Am J Med Genet. 1994. PMID: 8160735 Review.

10

Another case of spondylocostal dysplasia and severe anomalies.

Lin AE, Harster GA. Lin AE, et al. Am J Med Genet. 1993 Jun 1;46(4):476-7. doi: 10.1002/ajmg.1320460430. Am J Med Genet. 1993. PMID: 8357029 No abstract available.

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