Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 197

1.
2.

G syndrome: a review of the literature and a case report.

Bershof JF, Guyuron B, Olsen MM.

J Craniomaxillofac Surg. 1992 Jan;20(1):24-7. Review.

PMID:
1564117
3.

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.

PMID:
16186708
4.

The pattern of cardiovascular malformation in the CHARGE association.

Lin AE, Chin AJ, Devine W, Park SC, Zackai E.

Am J Dis Child. 1987 Sep;141(9):1010-3.

PMID:
2441595
5.

CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients.

Guion-Almeida ML, Richieri-Costa A.

Am J Med Genet. 1992 Aug 1;43(6):918-28.

PMID:
1415340
6.

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. doi: 10.1111/j.1447-0756.2010.01257.x.

PMID:
20666962
7.

The G syndrome/Opitz oculo-genital-laryngeal syndrome/Opitz BBB/G syndrome/Opitz-Frias syndrome.

Conlon BJ, O'Dwyer T.

J Laryngol Otol. 1995 Mar;109(3):244-6.

PMID:
7745346
8.

BBBG syndrome or Opitz syndrome: new family.

Verloes A, Le Merrer M, Briard ML.

Am J Med Genet. 1989 Nov;34(3):313-6. Review.

PMID:
2688419
9.

Noncardiac malformations in congenital heart disease: a retrospective analysis of 305 pediatric autopsies.

Güçer S, Ince T, Kale G, Akçören Z, Ozkutlu S, Talim B, Cağlar M.

Turk J Pediatr. 2005 Apr-Jun;47(2):159-66.

PMID:
16052857
10.

Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.

Leonardi ML, Pai GS, Wilkes B, Lebel RR.

Am J Med Genet. 2001 Aug 15;102(3):237-42. Review.

PMID:
11484200
11.

Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.

Reutter H, Bökenkamp A, Ebert AK, Rösch W, Boemers TM, Nöthen MM, Ludwig M.

Eur J Pediatr. 2009 Jul;168(7):881-3. doi: 10.1007/s00431-008-0852-5. Epub 2008 Oct 16. Review.

PMID:
18923839
12.

The CHARGE association in a newborn infant.

Akisü M, Ozkinay F, Ozyürek R, Küçüktaş A, Kültürsay N.

Turk J Pediatr. 1998 Apr-Jun;40(2):283-7.

PMID:
9714686
14.

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.

PMID:
1493644
15.

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 15;146A(18):2337-45. doi: 10.1002/ajmg.a.32368.

PMID:
18697196
16.

Ivemark syndrome in association with congenital septum transversum defect and pancreatic divisum.

Sharma S, Gangopadhyay AN, Sharma SP.

Indian J Gastroenterol. 2006 Mar-Apr;25(2):94-6.

PMID:
16763342
17.

Analysis of surgical outcome in complex double-outlet right ventricle with heterotaxy syndrome or complete atrioventricular canal defect.

Takeuchi K, McGowan FX Jr, Bacha EA, Mayer JE Jr, Zurakowski D, Otaki M, del Nido PJ.

Ann Thorac Surg. 2006 Jul;82(1):146-52.

PMID:
16798205
18.

Double aortic arch associated with common inlet left ventricle.

Kikuchi S, Yokozawa M.

Pediatr Cardiol. 2005 Jul-Aug;26(4):484-5.

PMID:
15690238
19.
20.

Chromosome 22q11 deletions in patients with conotruncal heart defects.

Khositseth A, Tocharoentanaphol C, Khowsathit P, Ruangdaraganon N.

Pediatr Cardiol. 2005 Sep-Oct;26(5):570-3.

PMID:
16132309

Supplemental Content

Support Center