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.
336 related articles for article (PubMed ID: 25851921)
21. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection. Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215 [TBL] [Abstract][Full Text] [Related]
22. Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings. Blanluet M; Chantot-Bastaraud S; Chambon P; Cassinari K; Vera G; Goldenberg A; Keren B; Le Meur N; Hannequin D; Mace B; Siffroi JP; Frebourg T; Nicolas G; Joly-Helas G Am J Med Genet A; 2021 Oct; 185(10):3057-3061. PubMed ID: 34043868 [TBL] [Abstract][Full Text] [Related]
23. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37). Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355 [TBL] [Abstract][Full Text] [Related]
24. 4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report. Wu M; Zheng X; Wang X; Zhang G; Kuang J BMC Med Genomics; 2020 Mar; 13(1):31. PubMed ID: 32126996 [TBL] [Abstract][Full Text] [Related]
25. Familial translocation t(10;14) (q26.1;q32.3): report of three offspring with 10q deletion and 14q duplication. Huang TH; Peckham D; Batanian JR; Martin MB; Kouba M; Caldwell CW; Miles JH Clin Genet; 1994 Oct; 46(4):299-303. PubMed ID: 7834895 [TBL] [Abstract][Full Text] [Related]
26. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11. Hu J; Sathanoori M; Kochmar S; Madan-Khetarpal S; McGuire M; Surti U Am J Med Genet A; 2013 Jan; 161A(1):179-84. PubMed ID: 23225375 [TBL] [Abstract][Full Text] [Related]
27. The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature. Torgyekes E; Shanske AL; Anyane-Yeboa K; Nahum O; Pirzadeh S; Blumfield E; Jobanputra V; Warburton D; Levy B Am J Med Genet A; 2011 Aug; 155A(8):1884-96. PubMed ID: 21744488 [TBL] [Abstract][Full Text] [Related]
28. Unbalanced cryptic 5p deletion/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5). Ensenauer R; Jalal S; Meyer R; Babovic-Vuksanovic D Am J Med Genet A; 2004 Feb; 125A(1):86-91. PubMed ID: 14755472 [TBL] [Abstract][Full Text] [Related]
29. Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20p. Oegema R; van Zutven LJ; van Hassel DA; Huijbregts GC; Hoogeboom AJ Eur J Med Genet; 2012 Apr; 55(4):265-8. PubMed ID: 22406089 [TBL] [Abstract][Full Text] [Related]
30. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation. Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651 [TBL] [Abstract][Full Text] [Related]
31. Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case. Tuğ E; Yirmibeş Karaoğuz M; Kayhan G; Ergün MA; Perçin FE Am J Med Genet A; 2014 Jul; 164A(7):1770-6. PubMed ID: 24677787 [TBL] [Abstract][Full Text] [Related]
32. Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication. Horbinski C; Carter EM; Heard PL; Sathanoori M; Hu J; Vockley J; Gunn S; Hale DE; Surti U; Cody JD Am J Med Genet A; 2008 Nov; 146A(22):2898-904. PubMed ID: 18932219 [TBL] [Abstract][Full Text] [Related]
33. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22). Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010 [TBL] [Abstract][Full Text] [Related]
34. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome. El-Ruby M; Hemly NA; Zaki MS Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874 [TBL] [Abstract][Full Text] [Related]
35. Deletion 2p15-16.1 syndrome: case report and review. Prontera P; Bernardini L; Stangoni G; Capalbo A; Rogaia D; Romani R; Ardisia C; Dallapiccola B; Donti E Am J Med Genet A; 2011 Oct; 155A(10):2473-8. PubMed ID: 21910216 [TBL] [Abstract][Full Text] [Related]
36. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization. Fritz B; Müller-Navia J; Hillig U; Köhler M; Aslan M; Rehder H Am J Med Genet; 1999 Dec; 87(4):297-301. PubMed ID: 10588833 [TBL] [Abstract][Full Text] [Related]
37. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH. Tyson C; McGillivray B; Chijiwa C; Rajcan-Separovic E Am J Med Genet A; 2004 Sep; 129A(3):254-60. PubMed ID: 15326624 [TBL] [Abstract][Full Text] [Related]
38. A Patient with Trisomy 4p and Monosomy 10q. Sobhani M; Tahmasbi P; Nasiri F; Rahnama M; Karimi-Nejad R; Tabatabaiefar MA Arch Iran Med; 2019 Jul; 22(7):414-417. PubMed ID: 31679386 [TBL] [Abstract][Full Text] [Related]
39. Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes. Sarri C; Douzgou S; Gyftodimou Y; Tümer Z; Ravn K; Pasparaki A; Sarafidou T; Kontos H; Kokotas H; Karadima G; Grigoriadou M; Pandelia E; Theodorou V; Moschonas NK; Petersen MB Am J Med Genet A; 2011 Nov; 155A(11):2841-54. PubMed ID: 21964744 [TBL] [Abstract][Full Text] [Related]
40. A patient with five chromosomal rearrangements and a 2q31.1 microdeletion. Wang T; Mao J; Liu MJ; Choy KW; Li HB; Cram DS; Li H; Chen Y Clin Chim Acta; 2014 Mar; 430():129-33. PubMed ID: 24412318 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]