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Results: 18

Related Articles by Review for PubMed (Select 16962354)

1.

Functional analysis of mutations in TGIF associated with holoprosencephaly.

El-Jaick KB, Powers SE, Bartholin L, Myers KR, Hahn J, Orioli IM, Ouspenskaia M, Lacbawan F, Roessler E, Wotton D, Muenke M.

Mol Genet Metab. 2007 Jan;90(1):97-111. Epub 2006 Sep 7. Review.

2.

Mutations in holoprosencephaly.

Wallis D, Muenke M.

Hum Mutat. 2000;16(2):99-108. Review.

PMID:
10923031
3.

Holoprosencephaly.

Dubourg C, Bendavid C, Pasquier L, Henry C, Odent S, David V.

Orphanet J Rare Dis. 2007 Feb 2;2:8. Review.

4.

Murine models of holoprosencephaly.

Schachter KA, Krauss RS.

Curr Top Dev Biol. 2008;84:139-70. doi: 10.1016/S0070-2153(08)00603-0. Review.

PMID:
19186244
5.

Mouse models of holoprosencephaly.

Hayhurst M, McConnell SK.

Curr Opin Neurol. 2003 Apr;16(2):135-41. Review.

PMID:
12644739
6.

Holoprosencephaly: clinical, anatomic, and molecular dimensions.

Cohen MM Jr.

Birth Defects Res A Clin Mol Teratol. 2006 Sep;76(9):658-73. Review.

PMID:
17001700
7.

Molecular mechanisms of holoprosencephaly.

Wallis DE, Muenke M.

Mol Genet Metab. 1999 Oct;68(2):126-38. Review.

PMID:
10527664
8.

Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in Brazil.

Richieri-Costa A, Ribeiro LA.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):149-57. doi: 10.1002/ajmg.c.30247. Review.

PMID:
20104612
9.

Molecular genetics of holoprosencephaly.

Nanni L, Schelper RL, Muenke MT.

Front Biosci. 2000 Mar 1;5:D334-42. Review.

10.

Holoprosencephaly: from Homer to Hedgehog.

Ming JE, Muenke M.

Clin Genet. 1998 Mar;53(3):155-63. Review.

PMID:
9630065
11.

Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients.

Pineda-Alvarez DE, Dubourg C, David V, Roessler E, Muenke M.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):93-101. doi: 10.1002/ajmg.c.30253. Review.

12.

Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE).

Mercier S, Dubourg C, Belleguic M, Pasquier L, Loget P, Lucas J, Bendavid C, Odent S.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):191-6. doi: 10.1002/ajmg.c.30246. Review.

PMID:
20104616
13.

Pathogenesis of holoprosencephaly.

Geng X, Oliver G.

J Clin Invest. 2009 Jun;119(6):1403-13. doi: 10.1172/JCI38937. Epub 2009 Jun 1. Review.

14.

Holoprosencephaly: An update on cytogenetic abnormalities.

Bendavid C, Dupé V, Rochard L, Gicquel I, Dubourg C, David V.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):86-92. doi: 10.1002/ajmg.c.30250. Review.

PMID:
20104602
15.

Role of TG-interacting factor (Tgif) in lipid metabolism.

Pramfalk C, Eriksson M, Parini P.

Biochim Biophys Acta. 2015 Jan;1851(1):9-12. doi: 10.1016/j.bbalip.2014.07.019. Epub 2014 Aug 1. Review.

PMID:
25088698
16.

The molecular genetics of holoprosencephaly.

Roessler E, Muenke M.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):52-61. doi: 10.1002/ajmg.c.30236. Review.

17.

Analysis of genotype-phenotype correlations in human holoprosencephaly.

Solomon BD, Mercier S, Vélez JI, Pineda-Alvarez DE, Wyllie A, Zhou N, Dubourg C, David V, Odent S, Roessler E, Muenke M.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):133-41. doi: 10.1002/ajmg.c.30240. Review.

18.

Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature.

Kauvar EF, Solomon BD, Curry CJ, van Essen AJ, Janssen N, Dutra A, Roessler E, Muenke M.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):158-69. doi: 10.1002/ajmg.c.30235. Review.

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