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.
310 related articles for article (PubMed ID: 9916836)
21. Familial ring (19) chromosome mosaicism: case report and review. Flejter WL; Finlinson D; Root S; Nguyen W; Brothman AR; Viskochil D Am J Med Genet; 1996 Dec; 66(3):276-80. PubMed ID: 8985487 [TBL] [Abstract][Full Text] [Related]
22. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate. Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553 [TBL] [Abstract][Full Text] [Related]
23. Mosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotype. Goossens E; Decock P; Potgieter S; Fryns JP Genet Couns; 1999; 10(2):133-6. PubMed ID: 10422005 [TBL] [Abstract][Full Text] [Related]
24. Molecular cytogenetic characterization of ring chromosome 4 in a female having a chromosomally normal child. Lee MH; Park SY; Kim YM; Kim JM; Yoo KJ; Lee HH; Ryu HM Cytogenet Genome Res; 2005; 111(2):175-8. PubMed ID: 16103661 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter). Syrrou M; Borghgraef M; Fryns JP Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044 [TBL] [Abstract][Full Text] [Related]
27. Characterization of two add(4qter) chromosomes by comparative genomic hybridization. Bocéno M; Rival JM; Nomballais MF; David A; Avet-Loiseau H Ann Genet; 1998; 41(2):83-6. PubMed ID: 9706338 [TBL] [Abstract][Full Text] [Related]
28. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development. Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571 [TBL] [Abstract][Full Text] [Related]
29. Cytogenetic studies in Down syndrome. Verma IC; Mathew S; Elango R; Shukla A Indian Pediatr; 1991 Sep; 28(9):991-6. PubMed ID: 1839389 [TBL] [Abstract][Full Text] [Related]
30. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype. Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518 [TBL] [Abstract][Full Text] [Related]
31. Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization. Zhao J; Gordon PL; Wilroy RS; Martens PR; Tarleton J; Shulman LP; Simpson JL; Elias S; Tharapel AT Am J Med Genet; 1995 May; 56(4):398-402. PubMed ID: 7604849 [TBL] [Abstract][Full Text] [Related]
32. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Iourov IY; Vorsanova SG; Liehr T; Monakhov VV; Soloviev IV; Yurov YB Cytogenet Genome Res; 2008; 121(3-4):302-6. PubMed ID: 18758177 [TBL] [Abstract][Full Text] [Related]
34. Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literature. Schubert R; Eggermann T; Hofstaetter C; von Netzer B; Knöpfle G; Schwanitz G Am J Med Genet; 2002 Jul; 110(3):278-82. PubMed ID: 12116238 [TBL] [Abstract][Full Text] [Related]
35. [Mosaic variant of the translocation form of syndrome 18q-]. Badalian LO; Dement'eva GM; Malygina NA; Mutovin GR; Petrukhin AS Genetika; 1981; 17(10):1867-71. PubMed ID: 7198075 [TBL] [Abstract][Full Text] [Related]
36. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia. Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352 [TBL] [Abstract][Full Text] [Related]
37. Three cases of mosaicism for balanced reciprocal translocations. Leegte B; Sikkema-Raddatz B; Hordijk R; Bouman K; van Essen T; Castedo S; de Jong B Am J Med Genet; 1998 Oct; 79(5):362-5. PubMed ID: 9779802 [TBL] [Abstract][Full Text] [Related]
38. Evidence by spectral karyotyping that 8q11.2 is nonrandomly involved in lipoblastoma. Chen Z; Coffin CM; Scott S; Meloni-Ehrig A; Shepard R; Issa B; Forsyth DR; Sandberg AA; Brothman AR; Lowichik A J Mol Diagn; 2000 May; 2(2):73-7. PubMed ID: 11272891 [TBL] [Abstract][Full Text] [Related]
39. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies. Kulharya AS; Lovell CM; Flannery DB Am J Med Genet; 2002 Dec; 113(4):367-70. PubMed ID: 12457409 [TBL] [Abstract][Full Text] [Related]
40. Molecular cytogenetic investigations in a novel complex variant of t(8;21)(q22;q22) with ins(15;21)(q15;q22.2q22.3) in a patient with AML-M2 subtype. Kokate P; Ahmad F; Dalvi R; Das BR; Mandava S Cancer Genet Cytogenet; 2008 Jul; 184(1):52-6. PubMed ID: 18558290 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]