138 related articles for article (PubMed ID: 9078418)
1. Overgrowth. Section VI. Genetic syndromes and other disorders associated with overgrowth.
Sotos JF
Clin Pediatr (Phila); 1997 Mar; 36(3):157-70. PubMed ID: 9078418
[No Abstract] [Full Text] [Related]
2. Overgrowth syndromes: an update.
Cohen MM
Adv Pediatr; 1999; 46():441-91. PubMed ID: 10645472
[No Abstract] [Full Text] [Related]
3. Prenatal findings and the genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome.
Chen CP
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):186-91. PubMed ID: 22795092
[TBL] [Abstract][Full Text] [Related]
4. Overgrowth. Section V. Syndromes and other disorders associated with overgrowth.
Sotos JF
Clin Pediatr (Phila); 1997 Feb; 36(2):89-103. PubMed ID: 9118595
[No Abstract] [Full Text] [Related]
5. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
Eggermann T
Horm Res; 2009 Apr; 71 Suppl 2():30-5. PubMed ID: 19407494
[TBL] [Abstract][Full Text] [Related]
6. Overgrowth syndromes: a classification.
Neri G; Moscarda M
Endocr Dev; 2009; 14():53-60. PubMed ID: 19293574
[TBL] [Abstract][Full Text] [Related]
7. [Segmental overgrowth syndromes and therapeutic strategies].
Venot Q; Canaud G
Med Sci (Paris); 2020 Mar; 36(3):235-242. PubMed ID: 32228842
[TBL] [Abstract][Full Text] [Related]
8. Advances in overgrowth syndromes: clinical classification to molecular delineation in Sotos syndrome and Beckwith-Wiedemann syndrome.
Cytrynbaum CS; Smith AC; Rubin T; Weksberg R
Curr Opin Pediatr; 2005 Dec; 17(6):740-6. PubMed ID: 16282780
[TBL] [Abstract][Full Text] [Related]
9. Genetic considerations in the prenatal diagnosis of overgrowth syndromes.
Vora N; Bianchi DW
Prenat Diagn; 2009 Oct; 29(10):923-9. PubMed ID: 19609940
[TBL] [Abstract][Full Text] [Related]
10. Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome.
Eggermann T; Eggermann K; Schönherr N
Trends Genet; 2008 Apr; 24(4):195-204. PubMed ID: 18329128
[TBL] [Abstract][Full Text] [Related]
11. Epigenetic deregulation of imprinting in congenital diseases of aberrant growth.
Delaval K; Wagschal A; Feil R
Bioessays; 2006 May; 28(5):453-9. PubMed ID: 16615080
[TBL] [Abstract][Full Text] [Related]
12. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
Enklaar T; Zabel BU; Prawitt D
Expert Rev Mol Med; 2006 Jul; 8(17):1-19. PubMed ID: 16842655
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis and perinatal management of the Beckwith-Wiedeman syndrome: a case and review.
Lodeiro JG; Byers JW; Chuipek S; Feinstein SJ
Am J Perinatol; 1989 Oct; 6(4):446-9. PubMed ID: 2675874
[TBL] [Abstract][Full Text] [Related]
14. Beckwith-Wiedemann Syndrome (BWS): a case report and literature review.
Ogundiran TO; Aghahowa ME; Brown BJ; Irabor DO
West Afr J Med; 2003; 22(1):101-2. PubMed ID: 12769320
[TBL] [Abstract][Full Text] [Related]
15. Beckwith-Wiedemann syndrome.
Weksberg R; Shuman C; Smith AC
Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
[TBL] [Abstract][Full Text] [Related]
16. [The Wiedemann-Beckwith syndrome and a congenital cataract].
Momtchilova M; Pelosse B; Laroche L; Vazquez MP
J Fr Ophtalmol; 2001 May; 24(5):479-81. PubMed ID: 11397983
[TBL] [Abstract][Full Text] [Related]
17. The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes.
Hughes-Benzie R; Allanson J; Hunter A; Cole T
J Med Genet; 1992 Dec; 29(12):928. PubMed ID: 1479609
[No Abstract] [Full Text] [Related]
18. Clinical and molecular overlap in overgrowth syndromes.
Baujat G; Rio M; Rossignol S; Sanlaville D; Lyonnet S; Le Merrer M; Munnich A; Gicquel C; Colleaux L; Cormier-Daire V
Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):4-11. PubMed ID: 16010674
[TBL] [Abstract][Full Text] [Related]
19. Overgrowth.
Verge CF; Mowat D
Arch Dis Child; 2010 Jun; 95(6):458-63. PubMed ID: 20371592
[TBL] [Abstract][Full Text] [Related]
20. A child with Beckwith-Wiedemann syndrome and posterior urethral valves.
Buyukcelik M; Satar N; Dursun H; Bayazit Y; Bayazit AK; Soran M; Noyan A; Anarat A
Genet Couns; 2005; 16(1):41-4. PubMed ID: 15844777
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]