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Results: 1 to 20 of 157

Related Citations for PubMed (Select 9916841)

1.

VACTERL manifestations in two generations of a family.

Nezarati MM, McLeod DR.

Am J Med Genet. 1999 Jan 1;82(1):40-2.

PMID:
9916841
2.

VACTERL association with a cleft hand.

Endoh N, Igawa HH, Sugihara T.

Congenit Anom (Kyoto). 2003 Sep;43(3):180-3.

PMID:
14684968
3.

VACTERL-H associated with central hypothyroidism: a case report.

Aliefendioglu D, Bademci G, Keskil S, Somuncu S, Misirlioglu E, Cakmak AM.

Genet Couns. 2007;18(3):331-5.

PMID:
18019375
4.

Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL association.

de Jong EM, Felix JF, Deurloo JA, van Dooren MF, Aronson DC, Torfs CP, Heij HA, Tibboel D.

Birth Defects Res A Clin Mol Teratol. 2008 Feb;82(2):92-7. doi: 10.1002/bdra.20437.

PMID:
18186125
5.

VACTERL with hydrocephalus: family with X-linked VACTERL-H.

Lomas FE, Dahlstrom JE, Ford JH.

Am J Med Genet. 1998 Feb 26;76(1):74-8. Review.

PMID:
9508070
6.

VACTERL-H with triphalangeal thumb and hypothyroidism in a female patient.

Vatansever U, Başaran UN, Güzel A, Acunaş B, Balci S.

Clin Dysmorphol. 2004 Jan;13(1):29-30.

PMID:
15127761
7.

Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome.

Rossbach HC, Sutcliffe MJ, Haag MM, Grana NH, Rossi AR, Barbosa JL.

Am J Med Genet. 1996 Jan 2;61(1):65-7.

PMID:
8741921
8.

Tibial developmental field defect is the most common lower limb malformation pattern in VACTERL association.

Castori M, Rinaldi R, Cappellacci S, Grammatico P.

Am J Med Genet A. 2008 May 15;146A(10):1259-66. doi: 10.1002/ajmg.a.32288. Review.

PMID:
18386801
9.

Developmental field defects: coming together of associations and sequences during blastogenesis.

Hersh JH, Angle B, Fox TL, Barth RF, Bendon RW, Gowans G.

Am J Med Genet. 2002 Jul 15;110(4):320-3.

PMID:
12116204
10.

Familial recurrence of tracheoesophageal fistula and associated malformations.

McMullen KP, Karnes PS, Moir CR, Michels VV.

Am J Med Genet. 1996 Jun 28;63(4):525-8.

PMID:
8826429
11.

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. doi: 10.1136/jmg.2008.060913.

PMID:
20452998
12.

VACTERL with the mitochondrial np 3243 point mutation.

Damian MS, Seibel P, Schachenmayr W, Reichmann H, Dorndorf W.

Am J Med Genet. 1996 Apr 24;62(4):398-403.

PMID:
8723071
13.

Thomas syndrome: potter sequence with cleft lip/palate and cardiac anomalies.

Zlotogora J, Ariel I, Ornoy A, Yagel S, Eidelman AI.

Am J Med Genet. 1996 Mar 29;62(3):224-6.

PMID:
8882777
14.

Tethered spinal cord and VACTERL association.

Kuo MF, Tsai Y, Hsu WM, Chen RS, Tu YK, Wang HS.

J Neurosurg. 2007 Mar;106(3 Suppl):201-4.

PMID:
17465385
15.

A population study of the VACTERL association: evidence for its etiologic heterogeneity.

Khoury MJ, Cordero JF, Greenberg F, James LM, Erickson JD.

Pediatrics. 1983 May;71(5):815-20.

PMID:
6835768
16.

Tracheal agenesis with multiple congenital anomalies: a case report.

Wang CM, Chen SJ, Lu JH, Hwang BT.

Zhonghua Yi Xue Za Zhi (Taipei). 1998 Jan;61(1):48-52.

PMID:
9509693
17.

Should chromosome breakage studies be performed in patients with VACTERL association?

Faivre L, Portnoï MF, Pals G, Stoppa-Lyonnet D, Le Merrer M, Thauvin-Robinet C, Huet F, Mathew CG, Joenje H, Verloes A, Baumann C.

Am J Med Genet A. 2005 Aug 15;137(1):55-8. Review.

PMID:
16015582
18.

Townes-Brocks syndrome.

König R, Schick U, Fuchs S.

Eur J Pediatr. 1990 Dec;150(2):100-3.

PMID:
2279502
19.

Pallister-Hall syndrome with stenosis of the cricoid cartilage and microphallus without hypopituitarism.

Stoll C, De Saint Martin A, Donato L, Alembik K, Sauvage P, Messer J.

Genet Couns. 2001;12(3):231-5. Erratum in: Genet Couns. 2002;13(1):69.

PMID:
11693785
20.

Prenatal diagnosis of VACTERL syndrome and partial caudal regression syndrome: a previously unreported association.

Gedikbasi A, Yararbas K, Yildirim G, Yildirim D, Arslan O, Gul A, Ceylan Y.

J Clin Ultrasound. 2009 Oct;37(8):464-6. doi: 10.1002/jcu.20590.

PMID:
19536863
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