Laxova R - Search Results

1

De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.

Legare JM, Sekhon GS, Laxova R. Legare JM, et al. Among authors: laxova r. Am J Med Genet. 1994 Nov 15;53(3):216-21. doi: 10.1002/ajmg.1320530304. Am J Med Genet. 1994. PMID: 7856655 Review.

2

Del(10)(q22.3q24.1) associated with juvenile polyposis.

Jacoby RF, Schlack S, Sekhon G, Laxova R. Jacoby RF, et al. Among authors: laxova r. Am J Med Genet. 1997 Jun 27;70(4):361-4. doi: 10.1002/(sici)1096-8628(19970627)70:4<361::aid-ajmg6>3.0.co;2-w. Am J Med Genet. 1997. PMID: 9182775

3

Waardenburg syndrome type I in a child with deletion (2) (q35q36.2).

Kirkpatrick SJ, Kent CM, Laxova R, Sekhon GS. Kirkpatrick SJ, et al. Among authors: laxova r. Am J Med Genet. 1992 Nov 15;44(5):699-700. doi: 10.1002/ajmg.1320440533. Am J Med Genet. 1992. PMID: 1481835 Review. No abstract available.

4

Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter.

Gregg RG, Metzenberg AB, Hogan K, Sekhon G, Laxova R. Gregg RG, et al. Among authors: laxova r. Genomics. 1991 Apr;9(4):701-6. doi: 10.1016/0888-7543(91)90363-j. Genomics. 1991. PMID: 1674730

5

Previously unrecognized congenital progeroid disorder.

Petty EM, Laxova R, Wiedemann HR. Petty EM, et al. Among authors: laxova r. Am J Med Genet. 1990 Mar;35(3):383-7. doi: 10.1002/ajmg.1320350314. Am J Med Genet. 1990. PMID: 2309786

6

Diagnostic criteria for Walker-Warburg syndrome.

Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M, et al. Dobyns WB, et al. Among authors: laxova r. Am J Med Genet. 1989 Feb;32(2):195-210. doi: 10.1002/ajmg.1320320213. Am J Med Genet. 1989. PMID: 2494887

7

Progressive neurologic deterioration in a nine-year-old white male.

Barness LA, Chandra S, Kling P, Laxova R, Allen DB, Gilbert-Barness E. Barness LA, et al. Among authors: laxova r. Am J Med Genet. 1990 Dec;37(4):489-503. doi: 10.1002/ajmg.1320370413. Am J Med Genet. 1990. PMID: 2260594 No abstract available.

8

Dubowitz syndrome: long-term follow-up of an original patient.

Hansen KE, Kirkpatrick SJ, Laxova R. Hansen KE, et al. Among authors: laxova r. Am J Med Genet. 1995 Jan 16;55(2):161-4. doi: 10.1002/ajmg.1320550205. Am J Med Genet. 1995. PMID: 7536394

9

A 7-year old white-male boy with progressive neurological deterioration.

Barness LA, Henry K, Kling P, Laxova R, Kaback M, Gilbert-Barness E. Barness LA, et al. Among authors: laxova r. Am J Med Genet. 1991 Sep 1;40(3):271-9. doi: 10.1002/ajmg.1320400305. Am J Med Genet. 1991. PMID: 1951428

10

The critical region on the human Xq.

Therman E, Laxova R, Susman B. Therman E, et al. Among authors: laxova r. Hum Genet. 1990 Oct;85(5):455-61. doi: 10.1007/BF00194216. Hum Genet. 1990. PMID: 2227929 Review.

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