Watson MS - Search Results

1

Acute lymphoblastic leukemia with an unusual t(8;14)(q11.2;q32): a Pediatric Oncology Group Study.

Kaleem Z, Shuster JJ, Carroll AJ, Borowitz MJ, Pullen DJ, Camitta BM, Zutter MM, Watson MS. Kaleem Z, et al. Among authors: watson ms. Leukemia. 2000 Feb;14(2):238-40. doi: 10.1038/sj.leu.2401675. Leukemia. 2000. PMID: 10673739 Review.

2

t(2;14)(p13;q32): a recurring abnormality in lymphocytic leukemia. A Pediatric Oncology Group study.

Watson MS, Land VJ, Carroll AJ, Pullen J, Borowitz MJ, Link MP, Amylon M, Behm FG. Watson MS, et al. Cancer Genet Cytogenet. 1992 Feb;58(2):121-4. doi: 10.1016/0165-4608(92)90096-q. Cancer Genet Cytogenet. 1992. PMID: 1551073

3

Trisomy 21 in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group study (8602).

Watson MS, Carroll AJ, Shuster JJ, Steuber CP, Borowitz MJ, Behm FG, Pullen DJ, Land VJ. Watson MS, et al. Blood. 1993 Nov 15;82(10):3098-102. Blood. 1993. PMID: 8219201 Free article.

4

Acute promyelocytic leukemia with additional chromosomal abnormalities and absence of Auer rods.

Kaleem Z, Watson MS, Zutter MM, Blinder MA, Hess JL. Kaleem Z, et al. Among authors: watson ms. Am J Clin Pathol. 1999 Jul;112(1):113-8. doi: 10.1093/ajcp/112.1.113. Am J Clin Pathol. 1999. PMID: 10396293

5

Translocations involving chromosome 12p11-13, methotrexate metabolism, and outcome in childhood B-progenitor cell acute lymphoblastic leukemia: a Pediatric Oncology Group study.

Whitehead VM, Vuchich MJ, Cooley L, Lauer SJ, Mahoney DH, Shuster JJ, Payment C, Bernstein ML, Akabutu JJ, Bowen T, Kamen BA, Watson MS, Look AT, Pullen DJ, Camitta B. Whitehead VM, et al. Among authors: watson ms. Clin Cancer Res. 1998 Jan;4(1):183-8. Clin Cancer Res. 1998. PMID: 9516969

6

Aneuploidy and the fragile X syndrome.

Watson MS, Breg WR, Pauls D, Brown WT, Carroll AJ, Howard-Peebles PN, Meryash D, Shapiro LR. Watson MS, et al. Am J Med Genet. 1988 May-Jun;30(1-2):115-21. doi: 10.1002/ajmg.1320300110. Am J Med Genet. 1988. PMID: 2972203

7

An 11-year-old boy with mosaic ring chromosome 6 and dilated aortic root.

Ivanovich JL, Watson MS, Whelan AJ. Ivanovich JL, et al. Among authors: watson ms. Am J Med Genet. 2001 Jan 15;98(2):182-4. doi: 10.1002/1096-8628(20010115)98:2<182::aid-ajmg1028>3.0.co;2-y. Am J Med Genet. 2001. PMID: 11223855

8

Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation.

Whelan AJ, Watson MS, Porter FD, Steiner RD. Whelan AJ, et al. Among authors: watson ms. Am J Med Genet. 1995 Dec 4;59(4):492-4. doi: 10.1002/ajmg.1320590416. Am J Med Genet. 1995. PMID: 8585570

9

Case of direct insertion within a chromosome 3 leading to a chromosome 3p duplication in an offspring.

Watson MS, Dowton SB, Rohrbaugh J. Watson MS, et al. Am J Med Genet. 1990 Jun;36(2):172-4. doi: 10.1002/ajmg.1320360209. Am J Med Genet. 1990. PMID: 2368804

10

Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects.

Dowton SB, Hing AV, Sheen-Kaniecki V, Watson MS. Dowton SB, et al. Among authors: watson ms. J Med Genet. 1997 May;34(5):414-7. doi: 10.1136/jmg.34.5.414. J Med Genet. 1997. PMID: 9152840 Free PMC article.

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