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.
166 related articles for article (PubMed ID: 8933340)
1. Two sibs with Wolf-Hirschhorn and DiGeorge deletions resulting from an unbalanced chromosome rearrangement, 45,XX/XY, der(4)t(4;22) (p16.3;q11.2) mat,-22. Reddy KS; Sulcova V; Siassi B J Med Genet; 1996 Oct; 33(10):852-5. PubMed ID: 8933340 [TBL] [Abstract][Full Text] [Related]
2. Unbalanced 15;22 translocation in a patient with manifestations of DiGeorge and velocardiofacial syndrome. Jaquez M; Driscoll DA; Li M; Emanuel BS; Hernandez I; Jaquez F; Lembert N; Ramirez J; Matalon R Am J Med Genet; 1997 May; 70(1):6-10. PubMed ID: 9129733 [TBL] [Abstract][Full Text] [Related]
3. Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11. Funke B; Edelmann L; McCain N; Pandita RK; Ferreira J; Merscher S; Zohouri M; Cannizzaro L; Shanske A; Morrow BE Am J Hum Genet; 1999 Mar; 64(3):747-58. PubMed ID: 10053009 [TBL] [Abstract][Full Text] [Related]
4. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization]. Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946 [TBL] [Abstract][Full Text] [Related]
5. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat. Qumsiyeh MB; Stevens CA Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287 [TBL] [Abstract][Full Text] [Related]
6. De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome. Vittas S; Efstathiou G; Tsakalidis C; Malamaki C; Antari V; Chatzitoliou E; Chatziioannidis I; Galli-Tsinopoulou A; Soubasi V Cytogenet Genome Res; 2019; 158(1):32-37. PubMed ID: 30799418 [TBL] [Abstract][Full Text] [Related]
7. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis. Driscoll DA; Salvin J; Sellinger B; Budarf ML; McDonald-McGinn DM; Zackai EH; Emanuel BS J Med Genet; 1993 Oct; 30(10):813-7. PubMed ID: 8230155 [TBL] [Abstract][Full Text] [Related]
8. Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation. Zimmermann-Bär U; Stallmach T; Riegel M; Wiedemann U; Fauchère JC; Binkert F; Kotzot D Prenat Diagn; 2000 Oct; 20(10):847-50. PubMed ID: 11038468 [TBL] [Abstract][Full Text] [Related]
9. Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat. Martsolf JT; Chase TR; Jalal SM; Wasdahl WA Clin Genet; 1987 Jun; 31(6):366-9. PubMed ID: 3621637 [TBL] [Abstract][Full Text] [Related]
10. Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183). Mulder MP; Wilke M; Langeveld A; Wilming LG; Hagemeijer A; van Drunen E; Zwarthoff EC; Riegman PH; Deelen WH; van den Ouweland AM Hum Genet; 1995 Aug; 96(2):133-41. PubMed ID: 7635459 [TBL] [Abstract][Full Text] [Related]
11. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects. Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164 [TBL] [Abstract][Full Text] [Related]
12. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci. Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989 [TBL] [Abstract][Full Text] [Related]
13. A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome. Zollino M; Lecce R; Selicorni A; Murdolo M; Mancuso I; Marangi G; Zampino G; Garavelli L; Ferrarini A; Rocchi M; Opitz JM; Neri G Eur J Hum Genet; 2004 Oct; 12(10):797-804. PubMed ID: 15241479 [TBL] [Abstract][Full Text] [Related]
14. Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome. Paskulin GA; Riegel M; Cotter PD; Kiss A; Rosa RF; Zen PR; Mombach R; Graziadio C Am J Med Genet A; 2009 Jun; 149A(6):1302-7. PubMed ID: 19449429 [TBL] [Abstract][Full Text] [Related]
15. Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother. Fryns JP; Smeets E; Devriendt K; Petit P Ann Genet; 1998; 41(2):73-6. PubMed ID: 9706336 [TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome. Zollino M; Di Stefano C; Zampino G; Mastroiacovo P; Wright TJ; Sorge G; Selicorni A; Tenconi R; Zappalà A; Battaglia A; Di Rocco M; Palka G; Pallotta R; Altherr MR; Neri G Am J Med Genet; 2000 Sep; 94(3):254-61. PubMed ID: 10995514 [TBL] [Abstract][Full Text] [Related]
17. De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia. Chen CP; Chern SR; Lee CC; Chen WL; Chen MH; Chang KM J Med Genet; 1998 Dec; 35(12):1050-3. PubMed ID: 9863609 [TBL] [Abstract][Full Text] [Related]
18. A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation. Goodship J; Curtis A; Cross I; Brown J; Emslie J; Wolstenholme J; Bhattacharya S; Burn J J Med Genet; 1992 Jul; 29(7):451-4. PubMed ID: 1640422 [TBL] [Abstract][Full Text] [Related]
19. DiGeorge anomaly and chromosome 10p deletions: one or two loci? Dasouki M; Jurecic V; Phillips JA; Whitlock JA; Baldini A Am J Med Genet; 1997 Nov; 73(1):72-5. PubMed ID: 9375926 [TBL] [Abstract][Full Text] [Related]
20. Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation. Holmes SE; Riazi MA; Gong W; McDermid HE; Sellinger BT; Hua A; Chen F; Wang Z; Zhang G; Roe B; Gonzalez I; McDonald-McGinn DM; Zackai E; Emanuel BS; Budarf ML Hum Mol Genet; 1997 Mar; 6(3):357-67. PubMed ID: 9147638 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]