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Familial papillary carcinoma of the thyroid.
Stoffer SS, Van Dyke DL, Bach JV, Szpunar W, Weiss L. Stoffer SS, et al. Am J Med Genet. 1986 Dec;25(4):775-82. doi: 10.1002/ajmg.1320250415. Am J Med Genet. 1986. PMID: 3789026
Subtelomere deletions and translocations are frequently familial.
Adeyinka A, Adams SA, Lorentz CP, Van Dyke DL, Jalal SM. Adeyinka A, et al. Am J Med Genet A. 2005 May 15;135(1):28-35. doi: 10.1002/ajmg.a.30675. Am J Med Genet A. 2005. PMID: 15810004
Malformation syndrome of duplication 12q24.1 leads to qter.
Melnyk AR, Weiss L, Van Dyke DL, Jarvi P. Melnyk AR, et al. Am J Med Genet. 1981;10(4):357-65. doi: 10.1002/ajmg.1320100408. Am J Med Genet. 1981. PMID: 7332029
Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case.
Bawle EV, Conard J, Van Dyke DL, Czarnecki P, Driscoll DA. Bawle EV, et al. Am J Med Genet. 1998 Oct 12;79(5):406-10. doi: 10.1002/(sici)1096-8628(19981012)79:5<406::aid-ajmg18>3.0.co;2-v. Am J Med Genet. 1998. PMID: 9779813 No abstract available.
Inverted duplication of 8p: ten new patients and review of the literature.
Feldman GL, Weiss L, Phelan MC, Schroer RJ, Van Dyke DL. Feldman GL, et al. Am J Med Genet. 1993 Sep 15;47(4):482-6. doi: 10.1002/ajmg.1320470410. Am J Med Genet. 1993. PMID: 8256810 Review.
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.
Berend SA, Feldman GL, McCaskill C, Czarnecki P, Van Dyke DL, Shaffer LG. Berend SA, et al. Am J Med Genet. 1999 Jan 29;82(3):275-81. doi: 10.1002/(sici)1096-8628(19990129)82:3<275::aid-ajmg15>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10215554
Stable ring chromosome 21: molecular and clinical definition of the lesion.
Falik-Borenstein TC, Pribyl TM, Pulst SM, Van Dyke DL, Weiss L, Chu ML, Kraus J, Marshak D, Korenberg JR. Falik-Borenstein TC, et al. Am J Med Genet. 1992 Jan 1;42(1):22-8. doi: 10.1002/ajmg.1320420107. Am J Med Genet. 1992. PMID: 1308361
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