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GE Graham

Research Profile

Concepts & Ideas

Disorders

Chemicals & Drugs

Geographic Areas

Physiology

Facies

Anatomy

Living Beings

Nuclear Family

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Co-author Network

Co-Publications
Name
1
Maarten Egeler
1
Brian Lowry
1
Linda MacLaren
1
Ethylin Jabs

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Publications

TOP 3
R Brian Lowry; Ethylin Jabs; GE Graham; J Gerritsen; J Fleming
Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.
GE Graham; L M Graham; P J Bridge; Linda MacLaren; M J Coppes; R Maarten Egeler
Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH).
GE Graham; J E Allanson
Congenital cholesteatoma and malformations of the facial nerve: rare manifestations of the BOR syndrome.

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All Publications

2001: R Brian Lowry; Ethylin Jabs; GE Graham; J Gerritsen; J Fleming
Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.
American journal of medical genetics 2001;104(2):112-9.
2000: GE Graham; L M Graham; P J Bridge; Linda MacLaren; M J Coppes; R Maarten Egeler
Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH).
Pediatric research 2000;48(2):227-32.
1999: GE Graham; J E Allanson
Congenital cholesteatoma and malformations of the facial nerve: rare manifestations of the BOR syndrome.
American journal of medical genetics 1999;86(1):20-6.

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