Steele MW - Search Results

1

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. Among authors: steele mw. Am J Med Genet. 1988 Nov;31(3):533-48. doi: 10.1002/ajmg.1320310308. Am J Med Genet. 1988. PMID: 3067575 Review.

2

Risk effect of maternal age in Pallister i(12p) syndrome.

Wenger SL, Steele MW, Yu WD. Wenger SL, et al. Among authors: steele mw. Clin Genet. 1988 Sep;34(3):181-4. doi: 10.1111/j.1399-0004.1988.tb02860.x. Clin Genet. 1988. PMID: 3180504

3

Clinical consequences of deletion 1p35.

Wenger SL, Steele MW, Becker DJ. Wenger SL, et al. Among authors: steele mw. J Med Genet. 1988 Apr;25(4):263. doi: 10.1136/jmg.25.4.263. J Med Genet. 1988. PMID: 3367353 Free PMC article.

4

Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion.

Wenger SL, Hanchett JM, Steele MW, Maier BV, Golden WL. Wenger SL, et al. Among authors: steele mw. Am J Med Genet. 1987 Dec;28(4):881-7. doi: 10.1002/ajmg.1320280413. Am J Med Genet. 1987. PMID: 3688026

5

Meiotic consequences of pericentric inversions of chromosome 13.

Wenger SL, Steele MW. Wenger SL, et al. Among authors: steele mw. Am J Med Genet. 1981;9(4):275-83. doi: 10.1002/ajmg.1320090403. Am J Med Genet. 1981. PMID: 7294066

6

Chromosomal abnormalities in a psychiatric population.

Lewis KE, Lubetsky MJ, Wenger SL, Steele MW. Lewis KE, et al. Among authors: steele mw. Am J Med Genet. 1995 Feb 27;60(1):53-4. doi: 10.1002/ajmg.1320600110. Am J Med Genet. 1995. PMID: 7485235

7

"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents.

Wenger SL, Steele MW, Boone LY, Lenkey SG, Cummins JH, Chen XQ. Wenger SL, et al. Among authors: steele mw. Am J Med Genet. 1995 Jan 2;55(1):47-52. doi: 10.1002/ajmg.1320550114. Am J Med Genet. 1995. PMID: 7702096

8

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

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: steele mw. 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

Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocation.

Donahue SP, Wenger SL, Steele MW, Gorin MB. Donahue SP, et al. Among authors: steele mw. Ophthalmic Paediatr Genet. 1993 Mar;14(1):17-21. doi: 10.3109/13816819309087618. Ophthalmic Paediatr Genet. 1993. PMID: 8345951

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