-
1
-
-
0001400172
-
-
Vinkin PJ, Bruyn GW, eds. Amsterdam: North Holland
-
De Myer W. In: Vinkin PJ, Bruyn GW, eds. Handbook of clinical neurology, Amsterdam: North Holland, 1977:431-78.
-
(1977)
Handbook of Clinical Neurology
, pp. 431-478
-
-
De Myer, W.1
-
2
-
-
0016773230
-
Holoprosencephaly: Birth data, genetic and demographic analyses of 30 families
-
Roach E, De Myer W, Conneally PM, et al. Holoprosencephaly: birth data, genetic and demographic analyses of 30 families. Birth Defects 1975;11:294-313.
-
(1975)
Birth Defects
, vol.11
, pp. 294-313
-
-
Roach, E.1
De Myer, W.2
Conneally, P.M.3
-
3
-
-
0016339826
-
Congenital malformations in singletons: Epidemiological survey
-
Myrianthopoulos NC, Chung CS. Congenital malformations in singletons: epidemiological survey. Birth Defects 1974;X(11):1-58.
-
(1974)
Birth Defects
, vol.10
, Issue.11
, pp. 1-58
-
-
Myrianthopoulos, N.C.1
Chung, C.S.2
-
5
-
-
0016989731
-
Cytogenetic variants in holoprosencephaly. Report of a case and review of the literature
-
Ming PM, Goodner DM, Park TS. Cytogenetic variants in holoprosencephaly. Report of a case and review of the literature. Am J Dis Child 1976;130:864-7.
-
(1976)
Am J Dis Child
, vol.130
, pp. 864-867
-
-
Ming, P.M.1
Goodner, D.M.2
Park, T.S.3
-
6
-
-
0011977665
-
Holoprosencephaly as a genetic model for craniofacial development
-
Muenke M. Holoprosencephaly as a genetic model for craniofacial development. Dev Biol 1994;5:293-301.
-
(1994)
Dev Biol
, vol.5
, pp. 293-301
-
-
Muenke, M.1
-
7
-
-
0024420306
-
Clinical, cytogenetic and molecular approaches to the genetic heterogeneity of holoprosencephaly
-
Muenke M. Clinical, cytogenetic and molecular approaches to the genetic heterogeneity of holoprosencephaly. Am J Med Genet 1989;34:237-45.
-
(1989)
Am J Med Genet
, vol.34
, pp. 237-245
-
-
Muenke, M.1
-
8
-
-
0024317567
-
Perspectives on holoprosencephaly. Part I. Epidemiology, genetics and syndromology
-
Cohen MM Jr. Perspectives on holoprosencephaly. Part I. Epidemiology, genetics and syndromology. Teratology 1989;40:211-35.
-
(1989)
Teratology
, vol.40
, pp. 211-235
-
-
Cohen Jr., M.M.1
-
9
-
-
0028023154
-
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity
-
Muenke M, Gurriere F, Bay C, et al. Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity. Proc Natl Acad Sci USA 1994;91:8102-6.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 8102-8106
-
-
Muenke, M.1
Gurriere, F.2
Bay, C.3
-
10
-
-
0024245673
-
Microcephaly, holoprosencephaly, hypokinesia: A second report of a new syndrome
-
Hockey A, Crowhurst J, Culity G. Microcephaly, holoprosencephaly, hypokinesia: a second report of a new syndrome. Prenat Diagn 1988;8:683-6.
-
(1988)
Prenat Diagn
, vol.8
, pp. 683-686
-
-
Hockey, A.1
Crowhurst, J.2
Culity, G.3
-
11
-
-
0020539602
-
Holoprosencephaly in infants of diabetic mothers
-
Barr M Jr, Hanson JW, Currey K, et al. Holoprosencephaly in infants of diabetic mothers. J Pediatr 1983;102:565-8.
-
(1983)
J Pediatr
, vol.102
, pp. 565-568
-
-
Barr Jr., M.1
Hanson, J.W.2
Currey, K.3
-
12
-
-
0002777386
-
-
Cuticchia AJ, Pearson PL, eds. Baltimore: Johns Hopkins University Press
-
Schinzel A, McKusick VA, Francomano C, et al. In: Cuticchia AJ, Pearson PL, eds. Human gene mapping. Baltimore: Johns Hopkins University Press, 1993:735-72.
-
(1993)
Human Gene Mapping
, pp. 735-772
-
-
Schinzel, A.1
McKusick, V.A.2
Francomano, C.3
-
13
-
-
0017741766
-
Holoprosencephaly in human embryos: Epidemiologic studies of 150 cases
-
Matsunaga E, Shiota K. Holoprosencephaly in human embryos: epidemiologic studies of 150 cases. Teratology 1977;16:216-72.
-
(1977)
Teratology
, vol.16
, pp. 216-272
-
-
Matsunaga, E.1
Shiota, K.2
-
14
-
-
0014329459
-
Autosomal trisomy syndromes: A detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome
-
Taylor AI. Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome. J Med Genet 1968;5:227-52.
-
(1968)
J Med Genet
, vol.5
, pp. 227-252
-
-
Taylor, A.I.1
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