Watson MS - Search Results

1

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

2

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

3

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

4

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.

5

Partial monosomy of distal 10q: three new cases and a review.

Waggoner DJ, Chow CK, Dowton SB, Watson MS. Waggoner DJ, et al. Among authors: watson ms. Am J Med Genet. 1999 Sep 3;86(1):1-5. Am J Med Genet. 1999. PMID: 10440820 Review.

6

Chromosome abnormalities in congenital heart disease.

Johnson MC, Hing A, Wood MK, Watson MS. Johnson MC, et al. Among authors: watson ms. Am J Med Genet. 1997 Jun 13;70(3):292-8. doi: 10.1002/(sici)1096-8628(19970613)70:3<292::aid-ajmg15>3.0.co;2-g. Am J Med Genet. 1997. PMID: 9188669

7

Congenital heart defect in a patient with deletion of chromosome 7q.

Tiller GE, Watson MS, Duncan LM, Dowton SB. Tiller GE, et al. Among authors: watson ms. Am J Med Genet. 1988 Feb;29(2):283-7. doi: 10.1002/ajmg.1320290206. Am J Med Genet. 1988. PMID: 3354600

8

Deletion of 1q in a patient with acrofacial dysostosis.

Waggoner DJ, Ciske DJ, Dowton SB, Watson MS. Waggoner DJ, et al. Among authors: watson ms. Am J Med Genet. 1999 Feb 12;82(4):301-4. doi: 10.1002/(sici)1096-8628(19990212)82:4<301::aid-ajmg5>3.0.co;2-j. Am J Med Genet. 1999. PMID: 10051162

9

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

10

Deletion within chromosome 22 is common in patients with absent pulmonary valve syndrome.

Johnson MC, Strauss AW, Dowton SB, Spray TL, Huddleston CB, Wood MK, Slaugh RA, Watson MS. Johnson MC, et al. Among authors: watson ms. Am J Cardiol. 1995 Jul 1;76(1):66-9. doi: 10.1016/s0002-9149(99)80803-0. Am J Cardiol. 1995. PMID: 7793407

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