72 related articles for article (PubMed ID: 23265720)
1. [VACTERL-H association with tibial agenesis. Expansion of the clinical phenotype?].
Salinas-Torres VM; Ramos-Márquez ME; Angulo-Castellanos E
An Pediatr (Barc); 2013 Aug; 79(2):125-7. PubMed ID: 23265720
[No Abstract] [Full Text] [Related]
2. [Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome].
Salinas-Torres VM; Ramos-Márquez ME; Serra-Ruiz L; Angulo-Castellanos E
Arch Argent Pediatr; 2012 Aug; 110(4):e67-71. PubMed ID: 22859335
[TBL] [Abstract][Full Text] [Related]
3. Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient.
Salinas-Torres VM
Acta Neurol Belg; 2016 Jun; 116(2):229-31. PubMed ID: 26194037
[No Abstract] [Full Text] [Related]
4. VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer.
Chen CP; Chang TY; Chen YY; Chern SR; Su JW; Wang W
Taiwan J Obstet Gynecol; 2013 Dec; 52(4):575-9. PubMed ID: 24411047
[TBL] [Abstract][Full Text] [Related]
5. X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.
Mikat B; Roll C; Schindler D; Gembruch U; Klempert I; Buiting K; Bramswig NC; Wieczorek D
Clin Dysmorphol; 2016 Apr; 25(2):73-6. PubMed ID: 26683739
[No Abstract] [Full Text] [Related]
6. Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOS.
Alter BP; Giri N
Am J Med Genet A; 2016 Jun; 170(6):1520-4. PubMed ID: 27028275
[TBL] [Abstract][Full Text] [Related]
7. X-linked VACTERL-H caused by deletion of exon 3 in FANCB: A case report.
Watanabe N; Tsutsumi S; Miyano Y; Sato H; Nagase S
Congenit Anom (Kyoto); 2018 Sep; 58(5):171-172. PubMed ID: 29232005
[No Abstract] [Full Text] [Related]
8. VACTERL with hydrocephalus: further delineation of the syndrome(s).
Evans JA; Stranc LC; Kaplan P; Hunter AG
Am J Med Genet; 1989 Oct; 34(2):177-82. PubMed ID: 2816994
[TBL] [Abstract][Full Text] [Related]
9. Poland's syndrome with radial aplasia of the hand.
De Smet L
Genet Couns; 2013; 24(1):57-9. PubMed ID: 23610865
[TBL] [Abstract][Full Text] [Related]
10. Congenital associated malformations in a sample of Jordanian patients with cleft lip and palate.
Rawashdeh MA; Jawdat Abu-Hawas B
J Oral Maxillofac Surg; 2008 Oct; 66(10):2035-41. PubMed ID: 18848099
[TBL] [Abstract][Full Text] [Related]
11. [Congenital malformations among the infants born at the Clinica Ostetricia e Ginecologica dell'Università di Pavia from 1956 to 1966].
Gilardi G; Zara C
Arch Ostet Ginecol; 1968; 73(4):511-36. PubMed ID: 4238009
[No Abstract] [Full Text] [Related]
12. [Statistical study of congenital malformations at the Institute of Pathology of the University of Milan during 1946-66].
Fundarò P; Rescaldani R; Puccetti U; Bratina G; Grigolato P
Folia Hered Pathol (Milano); 1968; ():89-111. PubMed ID: 5760558
[No Abstract] [Full Text] [Related]
13. Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?
Wessels MW; Kuchinka B; Heydanus R; Smit BJ; Dooijes D; de Krijger RR; Lequin MH; de Jong EM; Husen M; Willems PJ; Casey B
J Med Genet; 2010 May; 47(5):351-5. PubMed ID: 20452998
[TBL] [Abstract][Full Text] [Related]
14. [Lissencephaly syndrome].
Bitran H; Weinhouse E; Grief M; Zirkin H
Harefuah; 1983 Sep; 105(5-6):115-7. PubMed ID: 6654258
[No Abstract] [Full Text] [Related]
15. Living donor liver transplantation for congenital absence of the portal vein in a child with cardiac failure.
Sumida W; Kaneko K; Ogura Y; Tainaka T; Ono Y; Seo T; Kiuchi T; Ando H
J Pediatr Surg; 2006 Nov; 41(11):e9-e12. PubMed ID: 17101345
[TBL] [Abstract][Full Text] [Related]
16. VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
Porteous ME; Cross I; Burn J
Am J Med Genet; 1992 Aug; 43(6):1032-4. PubMed ID: 1415330
[TBL] [Abstract][Full Text] [Related]
17. Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases.
Adle-Biassette H; Saugier-Veber P; Fallet-Bianco C; Delezoide AL; Razavi F; Drouot N; Bazin A; Beaufrère AM; Bessières B; Blesson S; Bucourt M; Carles D; Devisme L; Dijoud F; Fabre B; Fernandez C; Gaillard D; Gonzales M; Jossic F; Joubert M; Laurent N; Leroy B; Loeuillet L; Loget P; Marcorelles P; Martinovic J; Perez MJ; Satge D; Sinico M; Tosi M; Benichou J; Gressens P; Frebourg T; Laquerrière A
Acta Neuropathol; 2013 Sep; 126(3):427-42. PubMed ID: 23820807
[TBL] [Abstract][Full Text] [Related]
18. Follow-up of infants with single umbilical artery.
Froehlich LA; Fujikura T
Pediatrics; 1973 Jul; 52(1):6-13. PubMed ID: 4724442
[No Abstract] [Full Text] [Related]
19. Incidence of congenital abnormalities in Cape Town.
Horner R; Lanzkowsky P
S Afr Med J; 1966 Feb; 40(8):171. PubMed ID: 5909197
[No Abstract] [Full Text] [Related]
20. Tibial aplasia--VACTERL association, a new syndrome?
Basel D; Goldblatt J
Clin Dysmorphol; 2000 Jul; 9(3):205-8. PubMed ID: 10955482
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]