Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 91

1.

Omphalocele in half-siblings.

Kapur S, Higgins JV, Scott-Emuakpor AB, Dolanski EA.

Clin Genet. 1980 Jul;18(1):88-90.

PMID:
7418258
2.

Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel.

Sommer A, Cutler EA, Cohen BL, Harper D, Backes C.

Am J Med Genet. 1977;1(1):59-63.

PMID:
610426
3.

Familial occurrence of omphalocele suggesting sex-linked inheritance.

Havalad S, Noblett H, Speidel BD.

Arch Dis Child. 1979 Feb;54(2):142-3.

4.

Omphalocele in three generations with autosomal dominant transmission.

Kanagawa SL, Begleiter ML, Ostlie DJ, Holcomb G, Drake W, Butler MG.

J Med Genet. 2002 Mar;39(3):184-5.

5.

Familial omphalocele: analysis of risk factors and case report.

DiLiberti JH.

Am J Med Genet. 1982 Nov;13(3):263-8. No abstract available.

PMID:
7180872
6.

[Omphalocele: hereditary disease with dominant transmission?].

Le Marec B, Roussey M, Bracq H, Babut JM.

J Genet Hum. 1979 Oct;27(3):259-62. French.

PMID:
536741
7.

[Unusual case of familial incidence of omphalocele].

Kucera J, Goetz P, AntalĂ­k J.

Cesk Pediatr. 1971 May;26(5):237-9. Czech. No abstract available.

PMID:
5559527
8.

Familial omphalocele: considerations in genetic counseling.

Pryde PG, Greb A, Isada NB, Johnson MB, Klein M, Evans MI.

Am J Med Genet. 1992 Nov 15;44(5):624-7. Review.

PMID:
1481822
9.

Familial omphalocele and recurrence risk.

Lurie IW, Ilyina HG.

Am J Med Genet. 1984 Feb;17(2):541-3. No abstract available.

PMID:
6702903
10.

Familial omphalocele.

Steele K, Nevin NC.

Ulster Med J. 1985 Oct;54(2):214-5. No abstract available.

11.

Dysmorphic facies, omphalocele, laryngeal and pharyngeal hypoplasia, spinal anomalies, and learning disabilities in a new dominant malformation syndrome.

Shprintzen RJ, Goldberg RB.

Birth Defects Orig Artic Ser. 1979;15(5B):347-53. No abstract available.

PMID:
526588
12.
13.

The changing face of gastroschisis and omphalocele in southeast Georgia.

Goldkrand JW, Causey TN, Hull EE.

J Matern Fetal Neonatal Med. 2004 May;15(5):331-5.

PMID:
15280125
15.

Otopalatodigital syndrome type II associated with omphalocele: report of three cases.

Young K, Barth CK, Moore C, Weaver DD.

Am J Med Genet. 1993 Feb 15;45(4):481-7.

PMID:
8465856
16.

Omphalocele in an infant with Cornelia de Lange syndrome.

Lemire EG.

Clin Dysmorphol. 2006 Oct;15(4):255-6.

PMID:
16957487
17.

Parity effect on preterm birth and growth outcomes among infants with isolated omphalocele.

Salihu HM, Emusu D, Sharma PP, Aliyu ZY, Oyelese Y, Druschel CM, Kirby RS.

Eur J Obstet Gynecol Reprod Biol. 2006 Sep-Oct;128(1-2):91-6. Epub 2005 Dec 7.

PMID:
16337727
19.

Concomitant occurrence of holoprosencephaly and omphalocele.

Chen CP.

Genet Couns. 2008;19(1):95-9. No abstract available.

PMID:
18564505
20.

Chromosomal anomalies in newborns with omphalocele.

St-Vil D, Shaw KS, Lallier M, Yazbeck S, Di Lorenzo M, Grignon A, Blanchard H.

J Pediatr Surg. 1996 Jun;31(6):831-4.

PMID:
8783116

Supplemental Content

Support Center