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Results: 1 to 20 of 24

1.

Segregation analysis in nonsyndromic holoprosencephaly.

Odent S, Le Marec B, Munnich A, Le Merrer M, Bonaïti-Pellié C.

Am J Med Genet. 1998 May 1;77(2):139-43.

PMID:
9605287
[PubMed - indexed for MEDLINE]
2.

Molecular genetics of holoprosencephaly.

Nanni L, Schelper RL, Muenke MT.

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

PMID:
10704430
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

Management of children with holoprosencephaly.

Levey EB, Stashinko E, Clegg NJ, Delgado MR.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):183-90. doi: 10.1002/ajmg.c.30254. Review.

PMID:
20104615
[PubMed - indexed for MEDLINE]
5.

Holoprosencephaly: an antenatally-diagnosed case series and subject review.

Lim AS, Lim TH, Kee SK, Chia P, Raman S, Eu EL, Lim JY, Tien SL.

Ann Acad Med Singapore. 2008 Jul;37(7):594-7. Review.

PMID:
18695774
[PubMed - indexed for MEDLINE]
Free Article
6.

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
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation.

Hahn JS, Barnes PD.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):120-32. doi: 10.1002/ajmg.c.30238. Review.

PMID:
20104607
[PubMed - indexed for MEDLINE]
9.

Holoprosencephaly: from Homer to Hedgehog.

Ming JE, Muenke M.

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

PMID:
9630065
[PubMed - indexed for MEDLINE]
10.

Genetic approaches to understanding brain development: holoprosencephaly as a model.

Muenke M, Cohen MM Jr.

Ment Retard Dev Disabil Res Rev. 2000;6(1):15-21. Review.

PMID:
10899793
[PubMed - indexed for MEDLINE]
11.

Embryonic holoprosencephaly: pathology and phenotypic variability.

Yamada S.

Congenit Anom (Kyoto). 2006 Dec;46(4):164-71. Review.

PMID:
17096815
[PubMed - indexed for MEDLINE]
12.

Familial lupus erythematosus. Clinical and immunologic features of 125 multiplex families.

Michel M, Johanet C, Meyer O, Francès C, Wittke F, Michel C, Arfi S, Tournier-Lasserve E, Piette JC; Group for Research on Auto-Immune Disorders (GRAID).

Medicine (Baltimore). 2001 May;80(3):153-8. Review.

PMID:
11388091
[PubMed - indexed for MEDLINE]
13.

Holoprosencephaly: new models, new insights.

Krauss RS.

Expert Rev Mol Med. 2007 Sep 24;9(26):1-17. Review.

PMID:
17888203
[PubMed - indexed for MEDLINE]
14.

Mutations in holoprosencephaly.

Wallis D, Muenke M.

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

PMID:
10923031
[PubMed - indexed for MEDLINE]
15.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
[PubMed - indexed for MEDLINE]
16.

Evaluation and management of children with holoprosencephaly.

Hahn JS, Plawner LL.

Pediatr Neurol. 2004 Aug;31(2):79-88. Review.

PMID:
15301825
[PubMed - indexed for MEDLINE]
17.

Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature.

Fernandez BA, Siegel-Bartelt J, Herbrick JA, Teshima I, Scherer SW.

Clin Genet. 2005 Oct;68(4):349-59. Review.

PMID:
16143022
[PubMed - indexed for MEDLINE]
18.

Holoprosencephaly: recommendations for diagnosis and management.

Kauvar EF, Muenke M.

Curr Opin Pediatr. 2010 Dec;22(6):687-95. doi: 10.1097/MOP.0b013e32833f56d5. Review.

PMID:
20859208
[PubMed - indexed for MEDLINE]
19.

Severe brain and limb defects with possible autosomal recessive inheritance: a series of six cases and review of the literature.

Labrune P, Trioche P, Fallet-Bianco C, Roume J, Narcy F, Le Merrer M.

Am J Med Genet. 1997 Dec 12;73(2):144-9. Review.

PMID:
9409864
[PubMed - indexed for MEDLINE]
20.

[Progressive course of idiopathic pulmonary fibrosis in 2 monozygotic twin sisters].

Thomas H, Costabel U.

Pneumologie. 1996 Sep;50(9):679-82. Review. German.

PMID:
9011872
[PubMed - indexed for MEDLINE]

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