SCOPUS 정보 검색 플랫폼

American Journal of Medical Genetics

Volumn 87, Issue 3, 1999, Pages 251-253

Frontonasal dysostosis in two successive generations

(3) Nevin, Norman C a Leonard, Alan G b Jones, Barry c

a ROYAL GROUP OF HOSPITALS TRUST (United Kingdom)

b ROYAL BELFAST HOSPITAL FOR SICK CHILDREN (United Kingdom)

c GREAT ORMOND STREET HOSPITAL (United Kingdom)

Author keywords

Autosomal dominant; Frontonasal dysostosis; X linked dominant inheritance

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLEFT FACE; CLEFT LIP NOSE; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL MALFORMATION; FEMALE; HUMAN; HYPERTELORISM; PRESCHOOL CHILD; PRIORITY JOURNAL; X CHROMOSOME DOMINANT INHERITANCE;

ABNORMALITIES, MULTIPLE; ADULT; BRAIN NEOPLASMS; CHILD, PRESCHOOL; CLEFT LIP; CORPUS CALLOSUM; DYSOSTOSES; FACIAL BONES; FEMALE; FRONTAL BONE; HAIR; HUMANS; HYPERTELORISM; LIPOMA; PHENOTYPE; SKULL;

EID: 0033607473 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/(SICI)1096-8628(19991126)87:3<251::AID-AJMG10>3.0.CO;2-G Document Type: Article

Times cited : (26)

References (10)

1
- 0015068752
- Frontonasal dysplasia (median cleft face syndrome): Comments on etiology and pathogenesis
- Cohen MM Jr, Sedano HO, Gorlin RJ, Jirásek JE. 1971. Frontonasal dysplasia (median cleft face syndrome): comments on etiology and pathogenesis. Birth Defects Orig Art Series 7:117-119.
- (1971) Birth Defects Orig Art Series , vol.7 , pp. 117-119
- Cohen M.M., Jr.¹ Sedano, H.O.² Gorlin, R.J.³ Jirásek, J.E.⁴

2
- 0023143520
- Frontonasal dysplasia associated with tetratology of Fallot
- De Moor MM, Baruch R, Human DG. 1987. Frontonasal dysplasia associated with tetratology of Fallot. J Med Genet 24:107-109.
- (1987) J Med Genet , vol.24 , pp. 107-109
- De Moor, M.M.¹ Baruch, R.² Human, D.G.³

3
- 0014136944
- The median cleft facial syndrome: Differential diagnosis of cranium bifidum occultum, hypertelorism and median cleft nose, face and palate
- DeMeyer W. 1967. The median cleft facial syndrome: differential diagnosis of cranium bifidum occultum, hypertelorism and median cleft nose, face and palate. Neurology 17:961-971.
- (1967) Neurology , vol.17 , pp. 961-971
- DeMeyer, W.¹

4
- 0027182358
- Frontonasal dysplasia in two successive generations
- Fryburg JS, Persing JA, Lin KY. 1993. Frontonasal dysplasia in two successive generations. Am J Med Genet 46:712-714.
- (1993) Am J Med Genet , vol.46 , pp. 712-714
- Fryburg, J.S.¹ Persing, J.A.² Lin, K.Y.³

5
- 0030122081
- Frontonasal dysplasia: Analysis of 21 cases and literature review
- Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Jr MM. 1996. Frontonasal dysplasia: analysis of 21 cases and literature review. Int J Oral Maxillofac Surg 25:91-97.
- (1996) Int J Oral Maxillofac Surg , vol.25 , pp. 91-97
- Guion-Almeida, M.L.¹ Richieri-Costa, A.² Saavedra, D.³ Cohen M.M., Jr.⁴

6
- 2842599112
- A new inheritable syndrome with frontonasal dysplasia and associated with extracranial anomalies
- August 1977, Montreal
- Reich EW, Cox RP, McCarthy JB, Becker MH. 1977. A new inheritable syndrome with frontonasal dysplasia and associated with extracranial anomalies [abstract]. Vth International Conference on Birth Defects, August 1977, Montreal.
- (1977) Vth International Conference on Birth Defects
- Reich, E.W.¹ Cox, R.P.² McCarthy, J.B.³ Becker, M.H.⁴

7
- 0014798883
- Frontonasal dysplasia
- Sedano HO, Cohen MM Jr, Jirásek J, Gorlin RJ. 1970. Frontonasal dysplasia. J Pediatr 76:906-913.
- (1970) J Pediatr , vol.76 , pp. 906-913
- Sedano, H.O.¹ Cohen M.M., Jr.² Jirásek, J.³ Gorlin, R.J.⁴

8
- 0023898135
- Frontonasal malformation as a field defect and in syndromic associations
- Sedano HO, Gorlin RJ. 1988. Frontonasal malformation as a field defect and in syndromic associations. Oral Surg Oral Med Oral Path 65:704-710.
- (1988) Oral Surg Oral Med Oral Path , vol.65 , pp. 704-710
- Sedano, H.O.¹ Gorlin, R.J.²

9
- 0022946296
- Frontonasal "dysplasia," cerebral anomalies, and polydactyly: Report of a new syndrome and discussion from a developmental field perspective
- Toriello HV, Radecki LL, Sharda J, Looyenga D, Mann R. 1986.Frontonasal "dysplasia," cerebral anomalies, and polydactyly: report of a new syndrome and discussion from a developmental field perspective. Am J Med Genet [Suppl] 2:89-96.
- (1986) Am J Med Genet , vol.2 , Issue.SUPPL. , pp. 89-96
- Toriello, H.V.¹ Radecki, L.L.² Sharda, J.³ Looyenga, D.⁴ Mann, R.⁵

10
- 0015720823
- Median facial cleft syndrome in half sisters: Dilemmas in genetic counselling
- Warkany J, Bofinger MK, Benton C. 1973. Median facial cleft syndrome in half sisters: dilemmas in genetic counselling. Teratology 8:273-285.
- (1973) Teratology , vol.8 , pp. 273-285
- Warkany, J.¹ Bofinger, M.K.² Benton, C.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.