Midline Skeletodental Morphology in Holoprosencephaly

Author:

Kjær Inger,Keeling Jean W.,Fischer Hansen Birgit,Becktor Karin B.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Oral Surgery

Reference20 articles.

1. W. H. Arnold, G. H. Sperber, and G. A. Machin .Craniofacial skeletal development in three human synophthalmic holoprosencephalic fetuses., Ann Anat, 1998 .180 :45 –53 .

2. O. Chisaka, and M. R. Capecchi .Regionally restricted developmental defects resulting from a targeted disruption of the mouse homeobox gene Hox-1.5., Nature, 1991 .350 :473 –490 .

3. M. M. Cohen, J. E. Jirásek, R. T. Guzman, R. J. Gorlin, and M. Q. Peterson .Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis., Birth Defects, 1971 .7 :125 –135 .

4. Myer W. De, W. Zemann, and C. G. Palmer .The face predicts the brain: diagnostic significance of medial facial anomalies for holoprosencephaly (arhinencephaly)., Pediatrics, 1964 .34 :256 –263 .

5. C. R. Fitz, Holoprosencephaly and related entities., Neuroradiology, 1983 .25 :225 –238 .

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