Taylor HA - Search Results

1

Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6.

Schroer RJ, Culp DM, Stevenson RE, Potts WE, Taylor HA, Simensen RJ. Schroer RJ, et al. Among authors: taylor ha. Clin Genet. 1980 Jul;18(1):83-7. doi: 10.1111/j.1399-0004.1980.tb01369.x. Clin Genet. 1980. PMID: 7418257

2

Fragile X syndrome in South Carolina.

Saul RA, Stevenson RE, Simensen RJ, Wilkes G, Alexander W, Taylor H. Saul RA, et al. J S C Med Assoc. 1982 Sep;78(9):475-7. J S C Med Assoc. 1982. PMID: 6958922 No abstract available.

3

Beta-galactosidase deficiency: prolonged survival in three patients following early central nervous system deterioration.

Stevenson RE, Taylor HA Jr, Parks SE. Stevenson RE, et al. Among authors: taylor ha jr. Clin Genet. 1978 Mar;13(3):305-13. doi: 10.1111/j.1399-0004.1978.tb01185.x. Clin Genet. 1978. PMID: 416929

4

A digitopalatal syndrome with associated anomalies of the heart, face, and skeleton.

Stevenson RE, Taylor HA Jr, Burton OM, Hearn HB 3rd. Stevenson RE, et al. Among authors: taylor ha jr. J Med Genet. 1980 Jun;17(3):238-42. doi: 10.1136/jmg.17.3.238. J Med Genet. 1980. PMID: 7401139 Free PMC article.

5

Aspartylglucosaminuria in the United States.

Hreidarsson S, Thomas GH, Valle DL, Stevenson RE, Taylor H, McCarty J, Coker SB, Green WR. Hreidarsson S, et al. Clin Genet. 1983 Jun;23(6):427-35. doi: 10.1111/j.1399-0004.1983.tb01977.x. Clin Genet. 1983. PMID: 6883788

6

Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22.

Schwartz CE, Stanislovitis P, Phelan MC, Klinger K, Taylor HA, Stevenson RE. Schwartz CE, et al. Among authors: taylor ha. Cytogenet Cell Genet. 1991;56(3-4):152-3. doi: 10.1159/000133073. Cytogenet Cell Genet. 1991. PMID: 2055109

7

Beta-galactosidase deficiency: studies of two patients with prolonged survival.

Taylor HA, Stevenson RE, Parks SE. Taylor HA, et al. Am J Med Genet. 1980;5(3):235-45. doi: 10.1002/ajmg.1320050304. Am J Med Genet. 1980. PMID: 6773417

8

Transport media for tissue specimens: a comparative study.

Potts WE, Saul RA, Riley SE, Stevenson RE, Taylor HA. Potts WE, et al. Among authors: taylor ha. Am J Med Genet. 1983 Jul;15(3):507-10. doi: 10.1002/ajmg.1320150317. Am J Med Genet. 1983. PMID: 6881217 No abstract available.

9

Cutis gyratum and acanthosis nigricans associated with other anomalies: a distinctive syndrome.

Stevenson RE, Ferlauto GJ, Taylor HA. Stevenson RE, et al. Among authors: taylor ha. J Pediatr. 1978 Jun;92(6):950-2. doi: 10.1016/s0022-3476(78)80371-0. J Pediatr. 1978. PMID: 660365 No abstract available.

10

Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile type.

Stevenson RE, Lubinsky M, Taylor HA, Wenger DA, Schroer RJ, Olmstead PM. Stevenson RE, et al. Among authors: taylor ha. Pediatrics. 1983 Oct;72(4):441-9. Pediatrics. 1983. PMID: 6889058

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