-
1
-
-
0003984923
-
-
Berlin: Springer-Verlag
-
David, D. J., Poswillo, D., and Simpson, D. The Craniosynostoses: Causes, Natural History, and Management. Berlin: Springer-Verlag, 1982.
-
(1982)
The Craniosynostoses: Causes, Natural History, and Management
-
-
David, D.J.1
Poswillo, D.2
Simpson, D.3
-
2
-
-
0025809466
-
Classification and pathologic anatomy of limb anomalies
-
Upton, J. Classification and pathologic anatomy of limb anomalies. Clin. Plast. Surg. 18: 321, 1991.
-
(1991)
Clin. Plast. Surg.
, vol.18
, pp. 321
-
-
Upton, J.1
-
3
-
-
0019957742
-
Pathological anatomy of the hands in Apert's syndrome
-
Green, S. M. Pathological anatomy of the hands in Apert's syndrome. J. Hand Surg. 7A: 450, 1982.
-
(1982)
J. Hand Surg.
, vol.7 A
, pp. 450
-
-
Green, S.M.1
-
4
-
-
0022577705
-
Early surgical intervention in Apert's syndactyly
-
Barot, L. R., and Caplan, H. S. Early surgical intervention in Apert's syndactyly. Plast. Reconstr. Surg. 77: 282, 1986.
-
(1986)
Plast. Reconstr. Surg.
, vol.77
, pp. 282
-
-
Barot, L.R.1
Caplan, H.S.2
-
5
-
-
0025780415
-
Syndactyly correction of the hand in Apert syndrome
-
Zuker, R. M., Cleland, H. J., and Haswell, T. Syndactyly correction of the hand in Apert syndrome. Clin. Plast. Surg. 18: 357, 1991.
-
(1991)
Clin. Plast. Surg.
, vol.18
, pp. 357
-
-
Zuker, R.M.1
Cleland, H.J.2
Haswell, T.3
-
6
-
-
0014812559
-
The hand and Apert's syndrome
-
Hoover, G. H., Flatt, A. E., and Weiss, M. W. The hand and Apert's syndrome. J. Bone Joint Surg. 52A: 878, 1970.
-
(1970)
J. Bone Joint Surg.
, vol.52 A
, pp. 878
-
-
Hoover, G.H.1
Flatt, A.E.2
Weiss, M.W.3
-
7
-
-
0000639930
-
Acrocephaly and scaphocephaly with symmetrically distributed malformations of the extremities
-
Park, E. A., and Powers, G. F. Acrocephaly and scaphocephaly with symmetrically distributed malformations of the extremities. Am. J. Dis. Child. 20: 235, 1920.
-
(1920)
Am. J. Dis. Child.
, vol.20
, pp. 235
-
-
Park, E.A.1
Powers, G.F.2
-
8
-
-
0015754808
-
Apert syndrome and palatal mucopolysaccharides
-
Solomon, L. M., Medenica, M., Prusansky, S., and Kreiborg, S. Apert syndrome and palatal mucopolysaccharides. Teratology 8: 287, 1973.
-
(1973)
Teratology
, vol.8
, pp. 287
-
-
Solomon, L.M.1
Medenica, M.2
Prusansky, S.3
Kreiborg, S.4
-
9
-
-
4243591280
-
The natural history of Apert syndrome, with speculations on pathogenesis
-
Kaye, C. I., Matalon, R., and Prusansky, S. The natural history of Apert syndrome, with speculations on pathogenesis (Abstract). Teratology 17: 28A, 1978.
-
(1978)
Teratology
, vol.17
-
-
Kaye, C.I.1
Matalon, R.2
Prusansky, S.3
-
10
-
-
0018115567
-
Progressive generalized bony dysplasia in Apert syndrome
-
Harris, V., Beligere, N., and Prusansky, S. Progressive generalized bony dysplasia in Apert syndrome. Birth Defects 14: 175, 1977.
-
(1977)
Birth Defects
, vol.14
, pp. 175
-
-
Harris, V.1
Beligere, N.2
Prusansky, S.3
-
11
-
-
0028798546
-
Apert Syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
-
Wilkie, A. O. M., Slaney, S. F., Oldridge, M., et al. Apert Syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genet. 9: 165, 1995.
-
(1995)
Nature Genet.
, vol.9
, pp. 165
-
-
Wilkie, A.O.M.1
Slaney, S.F.2
Oldridge, M.3
-
12
-
-
85177159540
-
Analysis of phenotypic features and FGFR2 mutations in Apert syndrome
-
in press
-
Park, W.-J., Theda, C., Maestri, N. E., et al. Analysis of phenotypic features and FGFR2 mutations in Apert syndrome. Am. J. Hum. Genet. (in press).
-
Am. J. Hum. Genet.
-
-
Park, W.-J.1
Theda, C.2
Maestri, N.E.3
-
13
-
-
0000939064
-
Role of movement in embryonic joint development
-
Drachmann, D. B., and Sokoloff, L. Role of movement in embryonic joint development. Dev. Biol. 14: 401, 1966.
-
(1966)
Dev. Biol.
, vol.14
, pp. 401
-
-
Drachmann, D.B.1
Sokoloff, L.2
-
16
-
-
0002595269
-
Normal Craniofacial Growth
-
M. M. Cohen, Jr. (Ed.), New York: Raven Press
-
Enlow, D. H. Normal Craniofacial Growth. In M. M. Cohen, Jr. (Ed.), Craniosynostosis:Diagnosis, Evaluation and Management. New York: Raven Press, 1986. P. 131.
-
(1986)
Craniosynostosis:Diagnosis, Evaluation and Management
, pp. 131
-
-
Enlow, D.H.1
-
17
-
-
0027522002
-
Skeletal abnormalities in Apert syndrome
-
Cohen, M. M., Jr., and Kreiborg, S. Skeletal abnormalities in Apert syndrome. Am. J. Med. Genet. 47: 624, 1993.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 624
-
-
Cohen Jr., M.M.1
Kreiborg, S.2
-
18
-
-
0000262192
-
The pathogenesis of premature cranial synostosis in man
-
Moss, M. L. The pathogenesis of premature cranial synostosis in man. Acta Anat. 37: 351, 1959.
-
(1959)
Acta Anat.
, vol.37
, pp. 351
-
-
Moss, M.L.1
-
19
-
-
0027234483
-
Comparative three dimensional analysis of CT scans of the calvaria and cranial base in Apert and Crouzon syndromes
-
Kreiborg, S., Marsh, J. L., Cohen, M. M., Jr., et al. Comparative three dimensional analysis of CT scans of the calvaria and cranial base in Apert and Crouzon syndromes. J. Craniomaxillofac. Surg. 21: 181, 1993.
-
(1993)
J. Craniomaxillofac. Surg.
, vol.21
, pp. 181
-
-
Kreiborg, S.1
Marsh, J.L.2
Cohen Jr., M.M.3
-
20
-
-
0017669453
-
Metacarpoplialangeal pattern profile analysis as a tool to identify gene carriers in the acrocephalosyndactyly syndromes
-
Escobar, V., and Bixler, D. Metacarpoplialangeal pattern profile analysis as a tool to identify gene carriers in the acrocephalosyndactyly syndromes. Birth Defects 13: 229, 1977.
-
(1977)
Birth Defects
, vol.13
, pp. 229
-
-
Escobar, V.1
Bixler, D.2
-
21
-
-
0029640960
-
Craniosynostoses: Phenotypic/molecular correlations
-
Cohen, M. M., Jr. Craniosynostoses: Phenotypic/molecular correlations. Am. J. Med. Genet. 56: 334, 1995.
-
(1995)
Am. J. Med. Genet.
, vol.56
, pp. 334
-
-
Cohen Jr., M.M.1
-
22
-
-
0028006789
-
Phenotypic variation in acrocephalosyndactyly syndromes: Unusual findings in a patient with features of Apert and Saethre-Chotzen syndromes
-
Cantrell, S. B., Moore, M. H., Trott, J. A., et al. Phenotypic variation in acrocephalosyndactyly syndromes: Unusual findings in a patient with features of Apert and Saethre-Chotzen syndromes. Cleft Palate Craniofac. J. 31: 487, 1994.
-
(1994)
Cleft Palate Craniofac. J.
, vol.31
, pp. 487
-
-
Cantrell, S.B.1
Moore, M.H.2
Trott, J.A.3
-
23
-
-
0025194360
-
Acrocephalospondylosyndactyly: A possible new syndrome. Analysis of the vertebral and intervertebral components
-
Wells, T. R., Falk, R. E., Senac, M. O., and Vachon, L. Acrocephalospondylosyndactyly: A possible new syndrome. Analysis of the vertebral and intervertebral components. Pediatr. Pathol. 10: 117, 1990.
-
(1990)
Pediatr. Pathol.
, vol.10
, pp. 117
-
-
Wells, T.R.1
Falk, R.E.2
Senac, M.O.3
Vachon, L.4
-
24
-
-
0029001825
-
Spinal anomalies in Pfeiffer syndrome
-
Moore, M. H., Lodge, M. L., and Clark, B. E. Spinal anomalies in Pfeiffer syndrome. Cleft Palate Craniofac. J. 32: 251, 1995.
-
(1995)
Cleft Palate Craniofac. J.
, vol.32
, pp. 251
-
-
Moore, M.H.1
Lodge, M.L.2
Clark, B.E.3
|