DeMyer, W.: A 46 chromosome cebocephaly, with remarks on the relation of 13-15 trisomy to holoprosencephaly (arhinencephaly). Ann Paediat.203: 169, 1964.
2.
Zeman, W. and Palmer, C.G.: The face predicts the brain; diagnostic significance of median facial anomalies for holoprosencephaly (arhinencephaly) . Pediatrics34: 256, 1964.
3.
—,— and —: Familial alobar holoprosencephaly (arhinencephaly) with median cleft lip and palate; report of patient with 46 chromosomes. Neurology13: 913, 1963.
4.
Haworth, J.C. , Medovy, H. and Lewis, A.J.: Cebocephaly with endocrine dysgenesis. J. Paediat.59: 726, 1961.
5.
Uchida, I.A. et al.: Familial short arm deficiency of chromosome 18 concomitant with arhinencephaly and alopecia congenita. Amer. J. Hum. Genet.17: 410, 1965.
6.
Marshall, R. et al.: Features of 13-15 trisomy syndrome with normal karyotype. Lancet1: 556, 1964.
7.
Landau, J.W. , Barry, J.M. and Koch, R.: Arhinencephaly. J. Pediat.62: 895, 1963.
8.
Ferrier, P., Widgren, S. and Ferrier, S.: Nonspecific pseudohermaphroditism. Helv. Paediat. Acta19: 1, 1964.
9.
Arey, L.B.: Developmental Anatomy, ed. 7. Philadelphia, W. B. Saunders Co., 1965, pp. 230, 472.
10.
Gorlin, R.J. , Yunis, J. and Anderson, V.E.: Short arm deletion of chromosome 18 in cebocephaly. Amer. J. Dis. Child.115: 473, 1968 .
11.
Conen, P.E. , Erkman, B. and Metaxotou, C.: The "D" syndrome. Ibid.111: 236, 1966.
12.
Grebe, H.: Zur Ätiologie der Arhinencephalie. Erbarzt12: 138, 1944.
13.
Hintz, R.L. , Menking, M. and Sotos, J.F.: Familial holoprosencephaly with endocrine dysgenesis. J. Pediat.72: 81, 1968.
