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Items: 1 to 20 of 122

1.

[Neuro-ophthalmological and genetic aspects of a family affected with Crouzon's cranio-facial dysostosis (author's transl)].

Bovard A, Klein D, Berney J, Ricci A, Brocher JE.

J Genet Hum. 1977 Mar;25(1):1-24. French. No abstract available.

PMID:
874461
2.

[Neuro-ophthalmological and genetic aspects of Crouzon's disease. Apropos of a familial case].

Bovard A, Klein D, Berney J, Ricci A, Brocher JE.

Rev Otoneuroophtalmol. 1977;49(5):373-8. French. No abstract available.

PMID:
607362
3.

[A case of cranio-facial dysostosis (Crouzon's disease) associated with hydrocephalus (author's transl)].

Kawai K, Shigemori M, In K, Kuga S, Kuramoto S.

No Shinkei Geka. 1980 Nov;8(11):1093-9. Japanese.

PMID:
7453940
4.

[A contribution on Crouzon's disease].

Pittke EC.

Klin Monbl Augenheilkd. 1983 Aug;183(2):122-7. German.

PMID:
6632678
5.

[Crouzon's disease (craniofacial dysostosis)].

Pukocz M, Hill L.

Klin Oczna. 1975 Apr;45(4):369-72. Polish. No abstract available.

PMID:
1121155
6.

[Morphologic changes of the facial bone structure in Crouzon's syndrome].

Fleischer-Peters A.

Fortschr Kieferorthop. 1971;32(3):379-86. German. No abstract available.

PMID:
5292039
7.

[Family with Crouzon's craniofacial dysostosis].

Vaillaud JC, Manassero J, Badach L.

J Genet Hum. 1974 Dec;22(4):381-7. French. No abstract available.

PMID:
4461765
8.

Bilateral keratoconus in Crouzon's syndrome.

Perlman JM, Zaidman GW.

Cornea. 1994 Jan;13(1):80-1.

PMID:
8131412
9.

[Hereditary craniofacial dysostosis and syndactylia. A contribution to the study of relations between Apert's disease and Crouzon's disease].

Alfieri A, Alù C, Ceccarini M.

J Genet Hum. 1968 Jan;16(3):1-13. French. No abstract available.

PMID:
4303974
10.
11.

Bilateral keratoconus in Crouzon's syndrome with unilateral acute hydrops.

Wolter JR.

J Pediatr Ophthalmol. 1977 May-Jun;14(3):141-3.

PMID:
915642
12.

Variable expressivity of Crouzon's syndrome within a family.

Kreiborg S, Jensen BL.

Scand J Dent Res. 1977 Mar;85(3):175-84.

PMID:
265609
13.

[Familial occurrence of Crouzon's disease].

Derkacz Z, Zaleski J.

Neurol Neurochir Pol. 1975 Nov-Dec;9(6):717-21. Polish.

PMID:
1202399
14.

[Hereditary craniofacial dysostosis (Crouzon's disease)].

Ludányi I, Bottlik G, Frey J.

Zentralbl Gynakol. 1971 May 1;93(18):617-22. German. No abstract available.

PMID:
4997980
15.

Crouzon's craniofacial dysostosis in Kenya.

Chana HS, Klauss V.

Br J Ophthalmol. 1988 Mar;72(3):196-7.

16.

Crouzon's disease (craniofacial dysostosis). A neuropsychiatric presentation.

Robertson MM, Reynolds HT.

S Afr Med J. 1975 Jan 4;49(1):7-10. No abstract available.

PMID:
1111138
17.
18.

[Cranio-metaphyseal dysplasia. Clinical and genetic study of a case].

Malpuech G, Raynaud EJ, Merle P, Jourde J, Espinasse G.

Arch Fr Pediatr. 1974 Jan;31(1):71-6. French. No abstract available.

PMID:
4842847
19.

Jackson-Weiss syndrome registered in four successive generations. The facies of Crouzon's syndrome with foot abnormalities.

Stanković B, Krstić V, Stankov B, Jojić L, Nagulić M, Artiko G.

Doc Ophthalmol. 1994;85(3):281-6.

PMID:
7924855
20.

[Familial occurrence of Crouzon's syndrome].

Tomaszewska B, Zoch-Zwierz W.

Wiad Lek. 1988 Jan 1;41(1):54-7. Polish. No abstract available.

PMID:
3407177
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