Holoprosencephaly

LE WE PMID CA

Holoprosencephaly

1217

Holoprosenzephalie

2002 1	Multiple hits during early embryonic development: digenic diseases and holoprosencephaly. [12395298] Am J Hum Genet 71(5): 1017-32 (2002)
2009 2	Pathogenesis of holoprosencephaly. [19487816] J Clin Invest 119(6): 1403-13 (2009)
2007 3	Holoprosencephaly. [17274816] Orphanet J Rare Dis 2(-): 8 (2007)
2000 4	Assessment of the deep gray nuclei in holoprosencephaly. [11110554] AJNR Am J Neuroradiol 21(10): 1955-61 (2000)
1999 5	Coexistent holoprosencephaly and Chiari II malformation. [10543640] AJNR Am J Neuroradiol 20(9): 1678-81 (1999)
2010 6	Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature. [20104614] Am J Med Genet C Semin Med Genet 154C(1): 176-82 (2010)
2010 7	The molecular genetics of holoprosencephaly. [20104595] Am J Med Genet C Semin Med Genet 154C(1): 52-61 (2010)
2010 8	Genesis of teratogen-induced holoprosencephaly in mice. [20104601] Am J Med Genet C Semin Med Genet 154C(1): 29-42 (2010)
2010 9	Roles of bone morphogenetic protein signaling and its antagonism in holoprosencephaly. [20104603] Am J Med Genet C Semin Med Genet 154C(1): 43-51 (2010)
2010 10	Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients. [20104604] Am J Med Genet C Semin Med Genet 154C(1): 93-101 (2010)
2010 11	Analysis of genotype-phenotype correlations in human holoprosencephaly. [20104608] Am J Med Genet C Semin Med Genet 154C(1): 133-41 (2010)
2010 12	Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literature. [20104609] Am J Med Genet C Semin Med Genet 154C(1): 170-5 (2010)
2010 13	Holoprosencephaly due to numeric chromosome abnormalities. [20104610] Am J Med Genet C Semin Med Genet 154C(1): 146-8 (2010)
2010 14	Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature. [20104613] Am J Med Genet C Semin Med Genet 154C(1): 158-69 (2010)
2007 15	Functional analysis of mutations in TGIF associated with holoprosencephaly. [16962354] Mol Genet Metab 90(1): 97-111 (2007)

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