119 related articles for article (PubMed ID: 2276740)
1. Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region.
Weksberg R; Glaves M; Teshima I; Waziri M; Patil S; Williams BR
Genomics; 1990 Dec; 8(4):693-8. PubMed ID: 2276740
[TBL] [Abstract][Full Text] [Related]
2. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.
Weksberg R; Teshima I; Williams BR; Greenberg CR; Pueschel SM; Chernos JE; Fowlow SB; Hoyme E; Anderson IJ; Whiteman DA
Hum Mol Genet; 1993 May; 2(5):549-56. PubMed ID: 8518793
[TBL] [Abstract][Full Text] [Related]
3. The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome.
Gessler M; Hameister H; Henry I; Junien C; Braun T; Arnold HH
Hum Genet; 1990 Dec; 86(2):135-8. PubMed ID: 2176177
[TBL] [Abstract][Full Text] [Related]
4. Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11.
Nyström A; Cheetham JE; Engström W; Schofield PN
Eur J Pediatr; 1992 Jul; 151(7):511-4. PubMed ID: 1356785
[TBL] [Abstract][Full Text] [Related]
5. Regional mapping of the parathyroid hormone gene (PTH) by cytogenetic and molecular studies.
Tonoki H; Narahara K; Matsumoto T; Niikawa N
Cytogenet Cell Genet; 1991; 56(2):103-4. PubMed ID: 1672845
[TBL] [Abstract][Full Text] [Related]
6. Molecular biology of Beckwith-Wiedemann syndrome.
Weksberg R; Squire JA
Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075
[TBL] [Abstract][Full Text] [Related]
7. Molecular findings in Beckwith-Wiedemann syndrome.
Choufani S; Shuman C; Weksberg R
Am J Med Genet C Semin Med Genet; 2013 May; 163C(2):131-40. PubMed ID: 23592339
[TBL] [Abstract][Full Text] [Related]
8. Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome.
Henry I; Jeanpierre M; Barichard F; Serre JL; Mallet J; Turleau C; de Grouchy J; Junien C
Ann Genet; 1988; 31(4):216-20. PubMed ID: 2905880
[TBL] [Abstract][Full Text] [Related]
9. Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma.
Henry I; Jeanpierre M; Couillin P; Barichard F; Serre JL; Journel H; Lamouroux A; Turleau C; de Grouchy J; Junien C
Hum Genet; 1989 Feb; 81(3):273-7. PubMed ID: 2921038
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
Engel JR; Smallwood A; Harper A; Higgins MJ; Oshimura M; Reik W; Schofield PN; Maher ER
J Med Genet; 2000 Dec; 37(12):921-6. PubMed ID: 11106355
[TBL] [Abstract][Full Text] [Related]
12. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
Slatter RE; Elliott M; Welham K; Carrera M; Schofield PN; Barton DE; Maher ER
J Med Genet; 1994 Oct; 31(10):749-53. PubMed ID: 7837249
[TBL] [Abstract][Full Text] [Related]
13. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
[TBL] [Abstract][Full Text] [Related]
14. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.
Mannens M; Hoovers JM; Redeker E; Verjaal M; Feinberg AP; Little P; Boavida M; Coad N; Steenman M; Bliek J
Eur J Hum Genet; 1994; 2(1):3-23. PubMed ID: 7913866
[TBL] [Abstract][Full Text] [Related]
15. Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome.
Grandjean V; Smith J; Schofield PN; Ferguson-Smith AC
Proc Natl Acad Sci U S A; 2000 May; 97(10):5279-84. PubMed ID: 10779549
[TBL] [Abstract][Full Text] [Related]
16. Uniparental paternal disomy in a genetic cancer-predisposing syndrome.
Henry I; Bonaiti-Pellié C; Chehensse V; Beldjord C; Schwartz C; Utermann G; Junien C
Nature; 1991 Jun; 351(6328):665-7. PubMed ID: 1675767
[TBL] [Abstract][Full Text] [Related]
17. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
[TBL] [Abstract][Full Text] [Related]
18. Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.
Spritz RA; Mager D; Pauli RM; Laxova R
Am J Hum Genet; 1986 Aug; 39(2):265-73. PubMed ID: 3529947
[TBL] [Abstract][Full Text] [Related]
19. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
Catchpoole D; Lam WW; Valler D; Temple IK; Joyce JA; Reik W; Schofield PN; Maher ER
J Med Genet; 1997 May; 34(5):353-9. PubMed ID: 9152830
[TBL] [Abstract][Full Text] [Related]
20. New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.
Smith AC; Rubin T; Shuman C; Estabrooks L; Aylsworth AS; McDonald MT; Steele L; Ray PN; Weksberg R
Cytogenet Genome Res; 2006; 113(1-4):313-7. PubMed ID: 16575195
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
