Seltzer WK - Search Results

1

Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndrome.

Cole DE, Clarke LA, Riddell DC, Samson KA, Seltzer WK, Salisbury S. Cole DE, et al. Among authors: seltzer wk. Clin Chem. 1994 Nov;40(11 Pt 1):2099-103. Clin Chem. 1994. PMID: 7955386

2

Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.

McCabe ER, Towbin J, Chamberlain J, Baumbach L, Witkowski J, van Ommen GJ, Koenig M, Kunkel LM, Seltzer WK. McCabe ER, et al. Among authors: seltzer wk. J Clin Invest. 1989 Jan;83(1):95-9. doi: 10.1172/JCI113890. J Clin Invest. 1989. PMID: 2536049 Free PMC article.

3

Muscle glycerol kinase in Duchenne dystrophy and glycerol kinase deficiency.

Seltzer WK, Angelini C, Dhariwal G, Ringel SP, McCabe ER. Seltzer WK, et al. Muscle Nerve. 1989 Apr;12(4):307-13. doi: 10.1002/mus.880120409. Muscle Nerve. 1989. PMID: 2549414

4

Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus.

Towbin JA, Wu DR, Chamberlain J, Larsen PD, Seltzer WK, McCabe ER. Towbin JA, et al. Among authors: seltzer wk. Hum Genet. 1989 Sep;83(2):122-6. doi: 10.1007/BF00286703. Hum Genet. 1989. PMID: 2550352

5

DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis.

Towbin JA, Chamberlain JS, Wu DR, Pillers DA, Seltzer WK, McCabe ER. Towbin JA, et al. Among authors: seltzer wk. Genomics. 1990 Jul;7(3):442-4. doi: 10.1016/0888-7543(90)90181-s. Genomics. 1990. PMID: 2163974

6

Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndrome.

Pillers DA, Seltzer WK, Powell BR, Ray PN, Tremblay F, La Roche GR, Lewis RA, McCabe ER, Eriksson AW, Weleber RG. Pillers DA, et al. Among authors: seltzer wk. Arch Ophthalmol. 1993 Nov;111(11):1558-63. doi: 10.1001/archopht.1993.01090110124037. Arch Ophthalmol. 1993. PMID: 8240114

7

Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Francke U, Harper JF, Darras BT, Cowan JM, McCabe ER, Kohlschütter A, Seltzer WK, Saito F, Goto J, Harpey JP, et al. Francke U, et al. Among authors: seltzer wk. Am J Hum Genet. 1987 Mar;40(3):212-27. Am J Hum Genet. 1987. PMID: 2883886 Free PMC article.

8

Adrenal dysfunction in glycerol kinase deficiency.

Seltzer WK, Firminger H, Klein J, Pike A, Fennessey P, McCabe ER. Seltzer WK, et al. Biochem Med. 1985 Apr;33(2):189-99. doi: 10.1016/0006-2944(85)90027-4. Biochem Med. 1985. PMID: 2988520 Review.

9

Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.

Schwartz LS, Tarleton J, Popovich B, Seltzer WK, Hoffman EP. Schwartz LS, et al. Among authors: seltzer wk. Am J Hum Genet. 1992 Oct;51(4):721-9. Am J Hum Genet. 1992. PMID: 1415217 Free PMC article.

10

Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome.

Burke BA, Wick MR, King R, Thompson T, Hansen J, Darrae BT, Francke U, Seltzer WK, McCabe ER, Scheithauer BW. Burke BA, et al. Among authors: seltzer wk. Am J Med Genet. 1988 Sep;31(1):75-97. doi: 10.1002/ajmg.1320310111. Am J Med Genet. 1988. PMID: 2906226 Review.

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