188 related articles for article (PubMed ID: 11038468)
1. 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]
2. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
[TBL] [Abstract][Full Text] [Related]
3. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
4. Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome.
Dufke A; Seidel J; Schöning M; Döbler-Neumann M; Kelbova C; Liehr T; Beensen V; Backsch C; Klein-Vogler U; Enders H
Cytogenet Cell Genet; 2000; 91(1-4):81-4. PubMed ID: 11173835
[TBL] [Abstract][Full Text] [Related]
5. Duplication 4p and deletion 4p (Wolf-Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation.
Takeno SS; Corbani M; Andrade JA; Smith Mde A; Brunoni D; Melaragno MI
Am J Med Genet A; 2004 Aug; 129A(2):180-3. PubMed ID: 15316961
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
Kohlschmidt N; Zielinski J; Brude E; Schäfer D; Olert J; Hallermann C; Coerdt W; Arnemann J
Prenat Diagn; 2000 Feb; 20(2):152-5. PubMed ID: 10694689
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of a fetus with unbalanced translocation (4;13)(p16;q32) with overlapping features of Patau and Wolf-Hirschhorn syndromes.
Tapper JK; Zhang S; Harirah HM; Panova NI; Merryman LS; Hawkins JC; Lockhart LH; Gei AB; Velagaleti GV
Fetal Diagn Ther; 2002; 17(6):347-51. PubMed ID: 12393964
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
South ST; Whitby H; Maxwell T; Aston E; Brothman AR; Carey JC
Am J Med Genet A; 2008 Oct; 146A(20):2691-7. PubMed ID: 18798325
[TBL] [Abstract][Full Text] [Related]
10. Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p.
Xu J; Freeman V; Carter RF; Paes B; Heshka T; Nowaczyk JM
Am J Med Genet; 2000 Aug; 93(4):285-9. PubMed ID: 10946354
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
Estabrooks LL; Rao KW; Korf B
Am J Med Genet; 1993 Jan; 45(1):97-100. PubMed ID: 8418669
[TBL] [Abstract][Full Text] [Related]
13. The Wolf-Hirschhorn syndrome in fetuses.
Tachdjian G; Fondacci C; Tapia S; Huten Y; Blot P; Nessmann C
Clin Genet; 1992 Dec; 42(6):281-7. PubMed ID: 1493641
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome.
Gandelman KY; Gibson L; Meyn MS; Yang-Feng TL
Am J Hum Genet; 1992 Sep; 51(3):571-8. PubMed ID: 1379774
[TBL] [Abstract][Full Text] [Related]
16. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
Wheeler PG; Weaver DD; Palmer CG
Am J Med Genet; 1995 Feb; 55(4):462-5. PubMed ID: 7762587
[TBL] [Abstract][Full Text] [Related]
17. Prenatal sonographic patterns in six cases of Wolf-Hirschhorn (4p-) syndrome.
Boog G; Le Vaillant C; Collet M; Dupré PF; Parent P; Bongain A; Benoit B; Trastour C
Fetal Diagn Ther; 2004; 19(5):421-30. PubMed ID: 15305099
[TBL] [Abstract][Full Text] [Related]
18. Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.
Zollino M; Lecce R; Murdolo M; Orteschi D; Marangi G; Selicorni A; Midro A; Sorge G; Zampino G; Memo L; Battaglia D; Petersen M; Pandelia E; Gyftodimou Y; Faravelli F; Tenconi R; Garavelli L; Mazzanti L; Fischetto R; Cavalli P; Savasta S; Rodriguez L; Neri G
Hum Genet; 2007 Dec; 122(5):423-30. PubMed ID: 17676343
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.
Dawson AJ; Mears AJ; Chudley AE; Bech-Hansen T; McDermid H
J Med Genet; 1996 Nov; 33(11):952-6. PubMed ID: 8950677
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
