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5. Partial distal 12q trisomy. de Muelenaere A, Fryns JP, Van Den Berghe H. Ann Genet; 1980 Jul; 23(4):251-3. PubMed ID: 6971608 [Abstract] [Full Text] [Related]
6. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome. Fryns JP, Kleczkowska A, Decock P, Van den Berghe H. Ann Genet; 1990 Jul; 33(1):46-8. PubMed ID: 2195981 [Abstract] [Full Text] [Related]
11. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation. Engelen JJ, de Die-Smulders CE, Dirckx R, Verhoeven WM, Tuinier S, Curfs LM, Hamers AJ. Am J Med Genet; 2002 Apr 22; 109(2):149-53. PubMed ID: 11977164 [Abstract] [Full Text] [Related]
16. de novo inversion-duplication of 2q35-2qter without growth retardation. Dahoun-Hadorn S, Bretton-Chappuis B. Ann Genet; 1992 Apr 22; 35(1):55-7. PubMed ID: 1610122 [Abstract] [Full Text] [Related]
17. A case of nondisjunction of chromosome 21 (47,X,Yqs,+21) in an Indian family with Yqs. Reddy KS, Thomas IM, Narayanan HS. Ann Genet; 1984 Apr 22; 27(3):194-6. PubMed ID: 6334487 [Abstract] [Full Text] [Related]
18. Supernumerary small chromosomal anomaly: report of three cases including one with a familial inversion of chromosome 5. Lee Ml, Schneider J, Wasant P, Yu CY, Trpis L, Liang YW, Lewis BM, Borkowf S, Borgaonkar DS. J Genet Hum; 1978 Sep 22; 26(3):275-85. PubMed ID: 739263 [Abstract] [Full Text] [Related]
19. An extra small submetacentric chromosome: possible partial 18 trisomy. Fujita K, Fujita HM. Jinrui Idengaku Zasshi; 1975 Mar 22; 19(4):371-5. PubMed ID: 1241595 [No Abstract] [Full Text] [Related]