160 related articles for article (PubMed ID: 1493644)
1. Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.
Fryns JP; Delooz J; van den Berghe H
Clin Genet; 1992 Dec; 42(6):314-6. PubMed ID: 1493644
[TBL] [Abstract][Full Text] [Related]
2. Clinical and molecular studies of patients with characteristics of Opitz G/BBB syndrome shows a novel MID1 mutation.
Hsieh EW; Vargervik K; Slavotinek AM
Am J Med Genet A; 2008 Sep; 146A(18):2337-45. PubMed ID: 18697196
[TBL] [Abstract][Full Text] [Related]
3. Case of polyhydramnios complicated by Opitz G/BBB syndrome.
Tajima H; Itoh H; Mochizuki A; Nakamura Y; Kobayashi Y; Hirai K; Suzuki K; Sugihara K; Ohishi A; Ohzeki T; Kanayama N
J Obstet Gynaecol Res; 2010 Aug; 36(4):876-81. PubMed ID: 20666962
[TBL] [Abstract][Full Text] [Related]
4. [Hypertelorism-hypospadias (BBB) syndrome. 2 additional family studies].
Krause M; Meinecke P; Krins M; Grote W
Monatsschr Kinderheilkd; 1990 Jan; 138(1):31-3. PubMed ID: 2314402
[TBL] [Abstract][Full Text] [Related]
5. Opitz BBBG syndrome: new family with late-onset, serious complication.
Schrander J; Schrander-Stumpel C; Berg J; Frias JL
Clin Genet; 1995 Aug; 48(2):76-9. PubMed ID: 7586655
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic overlap of the BBB and G syndromes.
Cordero JF; Holmes LB
Am J Med Genet; 1978; 2(2):145-52. PubMed ID: 263434
[TBL] [Abstract][Full Text] [Related]
7. A novel deletion in a Pearson syndrome infant with hypospadias and cleft lip and palate.
Lohi O; Kuusela AL; Arola M
J Inherit Metab Dis; 2005; 28(6):1165-6. PubMed ID: 16435219
[TBL] [Abstract][Full Text] [Related]
8. Multidisciplinary management of Opitz G BBB syndrome.
Parashar SY; Anderson PJ; Cox TC; McLean N; David DJ
Ann Plast Surg; 2005 Oct; 55(4):402-7. PubMed ID: 16186708
[TBL] [Abstract][Full Text] [Related]
9. Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations.
Migliore C; Athanasakis E; Dahoun S; Wonkam A; Lees M; Calabrese O; Connell F; Lynch SA; Izzi C; Pompilii E; Thakur S; van Maarle M; Wilson LC; Meroni G
Eur J Med Genet; 2013 Aug; 56(8):404-10. PubMed ID: 23791568
[TBL] [Abstract][Full Text] [Related]
10. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.
Quaderi NA; Schweiger S; Gaudenz K; Franco B; Rugarli EI; Berger W; Feldman GJ; Volta M; Andolfi G; Gilgenkrantz S; Marion RW; Hennekam RC; Opitz JM; Muenke M; Ropers HH; Ballabio A
Nat Genet; 1997 Nov; 17(3):285-91. PubMed ID: 9354791
[TBL] [Abstract][Full Text] [Related]
11. G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz-G" syndrome)--perspective in 1987 and bibliography.
Opitz JM
Am J Med Genet; 1987 Oct; 28(2):275-85. PubMed ID: 3322001
[No Abstract] [Full Text] [Related]
12. New cases of Bohring-Opitz syndrome, update, and critical review of the literature.
Bohring A; Oudesluijs GG; Grange DK; Zampino G; Thierry P
Am J Med Genet A; 2006 Jun; 140(12):1257-63. PubMed ID: 16691589
[TBL] [Abstract][Full Text] [Related]
13. Infantile high myopia in Bohring-Opitz syndrome.
Simpson AR; Gibbon CE; Quinn AG; Turnpenny PD
J AAPOS; 2007 Oct; 11(5):524-5. PubMed ID: 17498985
[TBL] [Abstract][Full Text] [Related]
14. [Variable expression of an autosomal dominant syndrome: (BBB syndrome or G syndrome)].
Le Merrer M; Verloes A; Narcy P; Briard ML
J Genet Hum; 1988 Jun; 36(3):257-64. PubMed ID: 3411306
[TBL] [Abstract][Full Text] [Related]
15. X-linked midline defects.
Toriello HV; Higgins JV
Am J Med Genet; 1985 May; 21(1):143-6. PubMed ID: 4039891
[TBL] [Abstract][Full Text] [Related]
16. Opitz GBBB syndrome and the 22q11.2 deletion.
Lacassie Y; Arriaza MI
Am J Med Genet; 1996 Mar; 62(3):318. PubMed ID: 8882795
[No Abstract] [Full Text] [Related]
17. Opitz oculo-genital-laryngeal syndrome (Opitz BBB/G compound syndrome).
Sedano HO; Gorlin RJ
Am J Med Genet; 1988 Jul; 30(3):847-9, 851. PubMed ID: 3189406
[No Abstract] [Full Text] [Related]
18. Three siblings with Robert's syndrome.
Zergollern L; Hitrec F
Clin Genet; 1976 Apr; 9(4):433-6. PubMed ID: 177235
[TBL] [Abstract][Full Text] [Related]
19. Surgical management of penoscrotal hypospadias in a child with Opitz G/BBB syndrome: a case report.
Ahmed F; Altam A; Alyhari Q; Badheeb M; Aljbri W; Al-Wageeh S; Al-Naggar A; Ghabisha S; Al-Shami E
Pan Afr Med J; 2023; 44():103. PubMed ID: 37250678
[TBL] [Abstract][Full Text] [Related]
20. Child with fronto-facio-nasal dysplasia, Hirschsprung's disease and hypospadias.
Fryer AE
Clin Dysmorphol; 1993 Apr; 2(2):120-2. PubMed ID: 8281272
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
