These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
382 related articles for article (PubMed ID: 2729354)
21. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques. Wolff DJ; Schwartz MF; Cohen MM; Schwartz S Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813 [TBL] [Abstract][Full Text] [Related]
22. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example. Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064 [TBL] [Abstract][Full Text] [Related]
23. Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies. Mohammed FM; Farag TI; Gunawardana SS; al-Digashim DD; al-Awadi SA; al-Othman SA; Sundareshan TS Am J Med Genet; 1989 Mar; 32(3):353-5. PubMed ID: 2729356 [TBL] [Abstract][Full Text] [Related]
24. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment. García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157 [TBL] [Abstract][Full Text] [Related]
25. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence. Lindgren V; Rosinsky B; Chin J; Berry-Kravis E Am J Med Genet; 1994 Jan; 49(1):67-73. PubMed ID: 8172253 [TBL] [Abstract][Full Text] [Related]
26. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome. Kitsiou-Tzeli S; Hallett JJ; Atkins L; Latt SA; Holmes LB Am J Med Genet; 1984 Aug; 18(4):725-9. PubMed ID: 6237580 [TBL] [Abstract][Full Text] [Related]
27. [Clinical case of tandem translocation between chromosomes 13 and 15]. Badalian LO; Arkhipov BA; Malygina NA; Patrukhin AS; Lysov VL Tsitol Genet; 1985; 19(4):304-8. PubMed ID: 4049521 [TBL] [Abstract][Full Text] [Related]
28. Chromosome 10qter deletion syndrome: a review and report of three new cases. Wulfsberg EA; Weaver RP; Cunniff CM; Jones MC; Jones KL Am J Med Genet; 1989 Mar; 32(3):364-7. PubMed ID: 2658586 [TBL] [Abstract][Full Text] [Related]
29. Brief clinical report: the dup(17p) syndrome. Feldman GM; Baumer JG; Sparkes RS Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295 [TBL] [Abstract][Full Text] [Related]
30. Isochromosome-formation in chromosome 9. Miller K; Arslan-Kirchner M Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983 [TBL] [Abstract][Full Text] [Related]
31. Robertsonian translocations and abnormal phenotypes. Groupe de Cytogénéticiens Français. Ann Genet; 1989; 32(1):5-9. PubMed ID: 2665630 [TBL] [Abstract][Full Text] [Related]
32. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation. Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413 [TBL] [Abstract][Full Text] [Related]
33. Duplication of 5q11.2----q13.1 from a familial (5;20) balanced insertion. Yip MY; Kemp J; Hanson N; Wilson M; Purvis-Smith S; Lam-Po-Tang PR Am J Med Genet; 1989 Jun; 33(2):220-3. PubMed ID: 2764031 [TBL] [Abstract][Full Text] [Related]
34. Clinical variability of partial duplication 1q: a clinical report and literature review. Rosenthal J; Abeliovich D; Carmi R Am J Med Genet; 1987 Aug; 27(4):787-92. PubMed ID: 3122569 [TBL] [Abstract][Full Text] [Related]
35. Duplication 7p de novo and literature review. Zerres K; Schwanitz G; Gellissen K; Schroers L; Sohler R Ann Genet; 1989; 32(4):225-9. PubMed ID: 2692511 [TBL] [Abstract][Full Text] [Related]
36. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature. Taysi K; Chao WT; Monaghan N; Monaco MP Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954 [TBL] [Abstract][Full Text] [Related]
37. [Trisomy of the short arm of chromosome 10p; description of a female patient with de novo duplication 10p11.2-15]. Fechtrup B; Kalhoff H; Diekmann L; Fritz B Klin Padiatr; 2000; 212(1):35-40. PubMed ID: 10719682 [TBL] [Abstract][Full Text] [Related]
38. Duplication of distal 19q: clinical report and review. Boyd E; Grass FS; Parke JC; Knutson K; Stevenson RE Am J Med Genet; 1992 Feb; 42(3):326-30. PubMed ID: 1536172 [TBL] [Abstract][Full Text] [Related]
39. Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome. Clementi M; Tenconi R; Turolla L; Silvan C; Bortotto L; Artifoni L Am J Med Genet; 1991 Nov; 41(2):246-50. PubMed ID: 1785643 [TBL] [Abstract][Full Text] [Related]
40. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies. Turleau C; Cabanis MO; Girault D; Ledeist F; Mettey R; Puissant H; Prieur M; de Grouchy J Am J Med Genet; 1989 Mar; 32(3):420-4. PubMed ID: 2729362 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]