Steele MW - Search Results

1

The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-).

Breg WR, Steele MW, Miller OJ, Warburton D, DeCapoa A, Allderdice PW. Breg WR, et al. Among authors: steele mw. J Pediatr. 1970 Nov;77(5):782-91. doi: 10.1016/s0022-3476(70)80236-0. J Pediatr. 1970. PMID: 5504069 No abstract available.

2

Chromosome analysis of human amniotic-fluid cells.

Steele MW, Breg WR Jr. Steele MW, et al. Lancet. 1966 Feb 19;1(7434):383-5. doi: 10.1016/s0140-6736(66)91387-0. Lancet. 1966. PMID: 4159775 No abstract available.

3

Letter: Renpenning's syndrome.

Steele MW, Chorazy AL. Steele MW, et al. Lancet. 1974 Apr 20;1(7860):752-3. doi: 10.1016/s0140-6736(74)92978-x. Lancet. 1974. PMID: 4132492 No abstract available.

4

Relaxation of imprinting in Prader-Willi syndrome.

Rogan PK, Seip JR, White LM, Wenger SL, Steele MW, Sperling MA, Menon R, Knoll JH. Rogan PK, et al. Among authors: steele mw. Hum Genet. 1998 Dec;103(6):694-701. doi: 10.1007/s004390050893. Hum Genet. 1998. PMID: 9921905

5

Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromes.

Wenger SL, Sell SL, Painter MJ, Steele MW. Wenger SL, et al. Among authors: steele mw. Am J Med Genet. 1997 May 16;70(2):150-4. Am J Med Genet. 1997. PMID: 9128934

6

Terminal 2q deletion--a recognizable syndrome.

Wenger SL, Boone LY, Surti U, Steele MW. Wenger SL, et al. Among authors: steele mw. Clin Genet. 1997 Apr;51(4):290. doi: 10.1111/j.1399-0004.1997.tb02475.x. Clin Genet. 1997. PMID: 9184258 No abstract available.

7

A simplified six-item checklist for screening for fragile X syndrome in the pediatric population.

Giangreco CA, Steele MW, Aston CE, Cummins JH, Wenger SL. Giangreco CA, et al. Among authors: steele mw. J Pediatr. 1996 Oct;129(4):611-4. doi: 10.1016/s0022-3476(96)70130-0. J Pediatr. 1996. PMID: 8859272

8

A molecular anatomical analysis of mosaic trisomy 16.

Greally JM, Neiswanger K, Cummins JH, Boone LY, Lenkey SG, Wenger SL, Lewis JL, Fischer D, Paul RA, Steele MW. Greally JM, et al. Among authors: steele mw. Hum Genet. 1996 Jul;98(1):86-90. doi: 10.1007/s004390050165. Hum Genet. 1996. PMID: 8682514

9

Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: clinical observations and genetic analysis.

Kobayashi M, Kaplan BS, Bellah RD, Sartore M, Rappaport E, Steele MW, Mansfield E, Gasparini P, Surrey S, Fortina P. Kobayashi M, et al. Among authors: steele mw. Am J Med Genet. 1995 Nov 6;59(2):218-24. doi: 10.1002/ajmg.1320590219. Am J Med Genet. 1995. PMID: 8588589

10

Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.

Scott JA, Wenger SL, Steele MW, Chakravarti A. Scott JA, et al. Among authors: steele mw. Am J Med Genet. 1995 Mar 13;56(1):67-71. doi: 10.1002/ajmg.1320560115. Am J Med Genet. 1995. PMID: 7747789

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