144 related articles for article (PubMed ID: 7318839)
1. The Weaver syndrome: a rare type of primordial overgrowth.
Majewski F; Ranke M; Kemperdick H; Schmidt E
Eur J Pediatr; 1981 Nov; 137(3):277-82. PubMed ID: 7318839
[TBL] [Abstract][Full Text] [Related]
2. Accelerated bone maturation syndrome of the Weaver type.
Weisswichert PH; Knapp G; Willich E
Eur J Pediatr; 1981 Nov; 137(3):329-33. PubMed ID: 7318847
[No Abstract] [Full Text] [Related]
3. A girl with the Weaver syndrome.
Thompson EM; Hill S; Leonard JV; Pembrey ME
J Med Genet; 1987 Apr; 24(4):232-4. PubMed ID: 3585940
[TBL] [Abstract][Full Text] [Related]
4. Twins and their mildly affected mother with Weaver syndrome.
Dumić M; Vuković J; Cvitkovic M; Medica I
Clin Genet; 1993 Dec; 44(6):338-40. PubMed ID: 8131308
[TBL] [Abstract][Full Text] [Related]
5. [Weaver syndrome. 1st case reported in Venezuela].
Sánchez O; Boufajreldin S; Oranges C; Orta C; Guerra D
Invest Clin; 1997 Mar; 38(1):9-24. PubMed ID: 9235073
[TBL] [Abstract][Full Text] [Related]
6. A new autosomal recessive disorder resembling Weaver syndrome.
Teebi AS; Sundareshan TS; Hammouri MY; al-Awadi SA; al-Saleh QA
Am J Med Genet; 1989 Aug; 33(4):479-82. PubMed ID: 2596508
[TBL] [Abstract][Full Text] [Related]
7. Weaver syndrome in two Japanese children.
Kondo I; Mori Y; Kuwajima K
Am J Med Genet; 1991 Nov; 41(2):221-4. PubMed ID: 1785638
[TBL] [Abstract][Full Text] [Related]
8. The syndromes of Marshall and Weaver.
Fitch N
J Med Genet; 1980 Jun; 17(3):174-8. PubMed ID: 7401127
[TBL] [Abstract][Full Text] [Related]
9. Further delineation of Weaver syndrome.
Ardinger HH; Hanson JW; Harrod MJ; Cohen MM; Tibbles JA; Welch JP; Young-Wee T; Sommer A; Goldberg R; Shprintzen RJ
J Pediatr; 1986 Feb; 108(2):228-35. PubMed ID: 2418189
[TBL] [Abstract][Full Text] [Related]
10. A Japanese male infant with the Weaver syndrome.
Kondo I; Mori Y; Kuwajima K
Jinrui Idengaku Zasshi; 1990 Sep; 35(3):257-62. PubMed ID: 2266602
[TBL] [Abstract][Full Text] [Related]
11. A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly.
Weaver DD; Graham CB; Thomas IT; Smith DW
J Pediatr; 1974 Apr; 84(4):547-52. PubMed ID: 4366187
[No Abstract] [Full Text] [Related]
12. Spectrum of NSD1 mutations in Sotos and Weaver syndromes.
Rio M; Clech L; Amiel J; Faivre L; Lyonnet S; Le Merrer M; Odent S; Lacombe D; Edery P; Brauner R; Raoul O; Gosset P; Prieur M; Vekemans M; Munnich A; Colleaux L; Cormier-Daire V
J Med Genet; 2003 Jun; 40(6):436-40. PubMed ID: 12807965
[TBL] [Abstract][Full Text] [Related]
13. [Acceleration of bone maturation and dysmorphic syndrome in 2 siblings (Marshall-Weaver syndrome)].
Jalaguier J; Montoya F; Germain M; Bonnet H
J Genet Hum; 1983 Dec; 31 Suppl 5():385-95. PubMed ID: 6674414
[TBL] [Abstract][Full Text] [Related]
14. Mental deficiency, alterations in performance, and CNS abnormalities in overgrowth syndromes.
Cohen MM
Am J Med Genet C Semin Med Genet; 2003 Feb; 117C(1):49-56. PubMed ID: 12561058
[TBL] [Abstract][Full Text] [Related]
15. Retarded skeletal maturation in Weaver syndrome.
Fretzayas A; Papanicolaou A; Tzanetakos K; Theodoridis C; Karpathios T
Acta Paediatr Scand; 1988 Nov; 77(6):930-2. PubMed ID: 3207030
[TBL] [Abstract][Full Text] [Related]
16. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
Weidle B; Orstavik KH
Tidsskr Nor Laegeforen; 1998 Apr; 118(10):1556-8. PubMed ID: 9615582
[TBL] [Abstract][Full Text] [Related]
17. Reply to "lymphoproliferative disorders in Sotos syndrome: observation in two cases".
Cole T; Allanson J
Am J Med Genet; 1998 Jan; 75(2):226-7. PubMed ID: 9450893
[No Abstract] [Full Text] [Related]
18. Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome.
van Asperen CJ; Overweg-Plandsoen WC; Cnossen MH; van Tijn DA; Hennekam RC
J Med Genet; 1998 Apr; 35(4):323-7. PubMed ID: 9598729
[TBL] [Abstract][Full Text] [Related]
19. Weaver's syndrome--primordial excessive growth velocity. A case report.
Dawood AA; Machado GT; Winship WS
S Afr Med J; 1985 Apr; 67(16):646-8. PubMed ID: 3983749
[TBL] [Abstract][Full Text] [Related]
20. Novel EED mutation in patient with Weaver syndrome.
Cooney E; Bi W; Schlesinger AE; Vinson S; Potocki L
Am J Med Genet A; 2017 Feb; 173(2):541-545. PubMed ID: 27868325
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]