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Results: 10

Related Articles by Review for PubMed (Select 477680)

1.
2.

Co-occurrence of severe Goltz-Gorlin syndrome and pentalogy of Cantrell - Case report and review of the literature.

Smigiel R, Jakubiak A, Lombardi MP, Jaworski W, Slezak R, Patkowski D, Hennekam RC.

Am J Med Genet A. 2011 May;155A(5):1102-5. doi: 10.1002/ajmg.a.33895. Epub 2011 Apr 11. Review.

PMID:
21484999
3.

Skeletal manifestations in Fryns syndrome.

Tsukahara M, Sase M, Tateishi H, Saito T, Kato H, Furukawa S.

Am J Med Genet. 1995 Jan 16;55(2):217-20. Review.

PMID:
7717421
4.

Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature.

Alessandri L, Brayer C, Attali T, Samperiz S, Tiran-Rajaofera I, Ramful D, Pilorget H.

Genet Couns. 2005;16(4):363-70. Review.

PMID:
16440878
5.

Sex reversal and diaphragmatic hernia in phenotypicaly female sibs with normal XY chromosomes.

Manouvrier-Hanu S, Besson R, Cousin L, Jeanpierre C, Kacet N, Cartigny M, Devisme L, Storme L, De Martinville B, Lequien P.

J Med Genet. 2000 Apr;37(4):315-8. Review. No abstract available.

6.

Incontinentia pigmenti (Bloch-Sulzberger syndrome).

Landy SJ, Donnai D.

J Med Genet. 1993 Jan;30(1):53-9. Review. No abstract available.

7.

MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome.

Happle R, Daniƫls O, Koopman RJ.

Am J Med Genet. 1993 Oct 1;47(5):710-3. Review.

PMID:
8267001
8.

Genodermatoses in women.

Mevorah B, Politi Y.

Clin Dermatol. 1997 Jan-Feb;15(1):17-29. Review. No abstract available.

PMID:
9034652
9.

Fryns syndrome survivors and neurologic outcome.

Van Hove JL, Spiridigliozzi GA, Heinz R, McConkie-Rosell A, Iafolla AK, Kahler SG.

Am J Med Genet. 1995 Nov 20;59(3):334-40. Review.

PMID:
8599357
10.

Congenital diaphragmatic hernia and pulmonary hypoplasia: new insights from developmental biology and genetics.

Ackerman KG, Pober BR.

Am J Med Genet C Semin Med Genet. 2007 May 15;145C(2):105-8. Review. No abstract available.

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