1. Dewald GW, Spurbeck JL. Sex chromosome anomalies associated with premature gonadal failure. Semin Reprod Endo 1983;1:79-92.

2. Dewald GW, Michels VV. Recurrent miscarriages: cytogenetic causes and genetic counseling of affected families. Clin Obst Gyn 1986;29:865-885.

3. Kuffel D, Zinsmeister A, Lindor N, Litzow M, Dewald GW. Mitomycin C chromosome stress test to identify hypersensitivity to bifunc-tional alkylating agents in patients with Fanconi anemia or aplastic anemia. Mayo Clin Proc 1997;72:579-580.

4. Dewald GW, Noonan KJ, Spurbeck JL, Johnson DD. T-lymphocytes and 7;14 translocations: frequency of occurrence, breakpoints, and clinical and biological significance. Am J Hum Genet 1986;38:520-532.

5. Dicken CH, Dewald GW, Gordon H. Sister chromatid exchanges in the Bloom syndrome. Arch Dermat 1978;114:755-760.

6. Lindor NM, Devries EMG, Michels VV, Schad CR, Jalal SM, Donovan KM, et al. Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo chromosome mosaicism. Clin Genet 1996;49:124-129.

7. Dewald GW, Schad CR, Lilla VC, Jalal SM. Frequency and photographs of HGM11 chromosome anomalies in bone marrow samples from 3,996 patients with malignant hematologic neoplasms. Can Genet Cytogenet 1993;68:60-69.

8. Dewald GW, Stupca P. 154 chromosome anomalies in hematologic malignancies. Leuk Res 2000;24:487-489.

9. Dewald GW, Morris MA, Lilla VC. Chromosome studies in neoplas-tic hematologic disorders. In: McClatchey KD, ed. Clinical Laboratory Medicine, Williams and Wilkens, Baltimore, MD, 1993, pp. 703-740.

10. Rex A, Preus M. A diagnostic index for Down syndrome. J Pediatr 1982;100:903-906.

11. Nagahana H, Haamoto Y, Takeuchi T. An autopsy case of the 18 trisomy syndrome. Bull Osaka Med Sch 1974;20:26-33.

12. Dewald G, Haymond MW, Spurbeck JL, Moore SB. Origin of chi 46,XX/46,XY chimerism in a human true hermaphrodite. Science 1980;207:321-323.

13. Niebuhr E. The cri du chat syndrome: epidemiology, cytogenetics, and clinical features. Hum Genet 1978;44:227-275.

14. Tachdjian G, Fondacci C, Tapia S, Huten Y, Blot P, Nessmann C. The Wolf-Hirschhorn syndrome in fetuses. Clin Genet 1992;42:281-287.

15. Fryns JP, Emmery L, Timmermans J, Pedersen JC, van den Berghe. Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5-year-old boy. Am J Hum Genet 1980;28:53-56.

16. Warburton D, Kline J, Stein Z, Hutzler M, Chin A, Hassold T. Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions. Am J Hum Genet 1987;41:465-483.

17. Lindor NM, Ney JA, Gaffey TA, Jenkins RB, Thibodeau SN, Dewald GW. A genetic review of complete and partial hydatidiform moles and nonmolar triploidy. Mayo Clin Proc 1992;67:791-799.

18. Dewald GW. Modern methods of chromosome analysis and their application in clinical practice. In: Homberger H, Batsakis JG, eds. Clinical Laboratory Annual, vol. 2, Appleton-Century Crofts, Nor-walk, CT, 1983, pp. 2:1-29.

19. Spurbeck JL, Carlson RO, Allen JE, Dewald GW. Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques. Can Genet Cytogenet 1988;32:59-66.

20. Dewald GW, Broderick DL, Tom WW, Hagstrom JE, Pierre RV. The efficacy of direct, 24-hour culture, and mitotic synchronization methods for cytogenetic analysis of bone marrow in neoplastic hematologic disorders. Can Genet Cytogenet 18:1-9, 1985.

21. Crifasi PA, Michels VV, Driscoll DJ, Jalal SM, Dewald GW. DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes. Mayo Clin Proc 1995;70:1148-1153.

22. Jalal SM, Law ME. Detection of newborn aneuploidy by interphase fluorescent in situ hybridization. Mayo Clin Proc 1997;72: 705-710.

23. Jalal SM, Law ME, Carlson RO, Dewald GW. Prenatal detection of aneuploidy by directly labeled multicolored probes and interphase fluorescence in situ hybridization. Mayo Clin Proc 1998;73:132-137.

24. Jalal SM, Law ME, Dewald GW. Atlas of Whole Chromosome Paint Probes: Normal Patterns and Utility for Abnormal Cases. Mayo Foundation for Medical Education and Research, Rochester, MN, 1996, 145 pp.

25. International system for cytogenetic nomenclature. Mitelman F, ed. S. Karger, Basel, 1995.

26. Kimmel DW, O'Fallon JR, Scheithauer BW, Kelly PJ, Dewald GW, Jenkins RB. Prognostic value of cytogenetic analysis in human cerebral astrocytomas. Ann Neur 1992;31:534-542.

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