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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

214 related items for PubMed ID: 25063195

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  • 22. Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
    Roessler E, Belloni E, Gaudenz K, Jay P, Berta P, Scherer SW, Tsui LC, Muenke M.
    Nat Genet; 1996 Nov; 14(3):357-60. PubMed ID: 8896572
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  • 27. PTCH mutations in four Brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI.
    Ribeiro LA, Murray JC, Richieri-Costa A.
    Am J Med Genet A; 2006 Dec 01; 140(23):2584-6. PubMed ID: 17001668
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  • 31. Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management.
    Malta M, AlMutiri R, Martin CS, Srour M.
    Children (Basel); 2023 Mar 30; 10(4):. PubMed ID: 37189898
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  • 36. Holoprosencephaly: from Homer to Hedgehog.
    Ming JE, Muenke M.
    Clin Genet; 1998 Mar 30; 53(3):155-63. PubMed ID: 9630065
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  • 37. Boc and Gas1 each form distinct Shh receptor complexes with Ptch1 and are required for Shh-mediated cell proliferation.
    Izzi L, Lévesque M, Morin S, Laniel D, Wilkes BC, Mille F, Krauss RS, McMahon AP, Allen BL, Charron F.
    Dev Cell; 2011 Jun 14; 20(6):788-801. PubMed ID: 21664577
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