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Year | Number of Results |
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1990 | 1 |
2001 | 1 |
2009 | 1 |
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Problems in the definition of holoprosencephaly.
Am J Med Genet. 2001 Oct 15;103(3):183-7. doi: 10.1002/ajmg.1546.abs.
Am J Med Genet. 2001.
PMID: 11745988
Review.
No abstract available.
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Mercier S, Dubourg C, Garcelon N, Campillo-Gimenez B, Gicquel I, Belleguic M, Ratié L, Pasquier L, Loget P, Bendavid C, Jaillard S, Rochard L, Quélin C, Dupé V, David V, Odent S.
Mercier S, et al.
J Med Genet. 2011 Nov;48(11):752-60. doi: 10.1136/jmedgenet-2011-100339. Epub 2011 Sep 22.
J Med Genet. 2011.
PMID: 21940735
Free PMC article.
Item in Clipboard
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
Lacbawan F, Solomon BD, Roessler E, El-Jaick K, Domené S, Vélez JI, Zhou N, Hadley D, Balog JZ, Long R, Fryer A, Smith W, Omar S, McLean SD, Clarkson K, Lichty A, Clegg NJ, Delgado MR, Levey E, Stashinko E, Potocki L, Vanallen MI, Clayton-Smith J, Donnai D, Bianchi DW, Juliusson PB, Njølstad PR, Brunner HG, Carey JC, Hehr U, Müsebeck J, Wieacker PF, Postra A, Hennekam RC, van den Boogaard MJ, van Haeringen A, Paulussen A, Herbergs J, Schrander-Stumpel CT, Janecke AR, Chitayat D, Hahn J, McDonald-McGinn DM, Zackai EH, Dobyns WB, Muenke M.
Lacbawan F, et al.
J Med Genet. 2009 Jun;46(6):389-98. doi: 10.1136/jmg.2008.063818. Epub 2009 Apr 2.
J Med Genet. 2009.
PMID: 19346217
Free PMC article.
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Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.
Corsello G, Buttitta P, Cammarata M, Lo Presti A, Maresi E, Zumpani L, Giuffrè L.
Corsello G, et al.
Am J Med Genet. 1990 Oct;37(2):244-9. doi: 10.1002/ajmg.1320370216.
Am J Med Genet. 1990.
PMID: 2147361
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