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Year | Number of Results |
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1997 | 1 |
1998 | 1 |
2001 | 1 |
2011 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 5000
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Mutations in the pre-replication complex cause Meier-Gorlin syndrome.
Nat Genet. 2011 Feb 27;43(4):356-9. doi: 10.1038/ng.775.
Nat Genet. 2011.
PMID: 21358632
Free PMC article.
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.
Guernsey DL, Matsuoka M, Jiang H, Evans S, Macgillivray C, Nightingale M, Perry S, Ferguson M, LeBlanc M, Paquette J, Patry L, Rideout AL, Thomas A, Orr A, McMaster CR, Michaud JL, Deal C, Langlois S, Superneau DW, Parkash S, Ludman M, Skidmore DL, Samuels ME.
Guernsey DL, et al.
Nat Genet. 2011 Feb 27;43(4):360-4. doi: 10.1038/ng.777.
Nat Genet. 2011.
PMID: 21358631
Item in Clipboard
Meier-Gorlin syndrome: report of eight additional cases and review.
Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV.
Bongers EM, et al.
Am J Med Genet. 2001 Aug 1;102(2):115-24. doi: 10.1002/ajmg.1452.
Am J Med Genet. 2001.
PMID: 11477602
Review.
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Assignment of the homologue of the yeast origin recognition complex subunit ORC4 (ORC4L) to human chromosome band 2q22-->q23 by in situ hybridization and somatic cell hybrid analysis.
Eki T, Dean FB, Kohda A, Okumura K, Abe M, Murakami Y, Ishiai M, Satomoto K, Hurwitz J, O'Donnell M, Hanaoka F.
Eki T, et al.
Cytogenet Cell Genet. 1998;81(1):89-90. doi: 10.1159/000014997.
Cytogenet Cell Genet. 1998.
PMID: 9691185
No abstract available.
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Identification of HsORC4, a member of the human origin of replication recognition complex.
Quintana DG, Hou Zh, Thome KC, Hendricks M, Saha P, Dutta A.
Quintana DG, et al.
J Biol Chem. 1997 Nov 7;272(45):28247-51. doi: 10.1074/jbc.272.45.28247.
J Biol Chem. 1997.
PMID: 9353276
Free article.
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