BIOMAT Database Logo BIOMAT Database Logo

Familial leukemia and osteogenesis imperfecta. 1967

G S Gilchrist, and N A Shore

UI MeSH Term Description Entries
D007945 Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. Leukemia, Lymphocytic,Lymphocytic Leukemia,Lymphoid Leukemia,Leukemias, Lymphocytic,Leukemias, Lymphoid,Lymphocytic Leukemias,Lymphoid Leukemias
D010013 Osteogenesis Imperfecta COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I. Fragilitas Ossium,Lobstein Disease,Brittle Bone Disease,Lobstein's Disease,Osteogenesis Imperfecta Tarda,Osteogenesis Imperfecta with Blue Sclerae,Osteogenesis Imperfecta, Type 1,Osteogenesis Imperfecta, Type I,Disease, Lobstein,Disease, Lobstein's,Lobsteins Disease,Ossiums, Fragilitas,Osteogenesis Imperfecta Tardas
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

G S Gilchrist, and N A Shore
Familial aminoaciduria in osteogenesis imperfecta.
September 1962, JAMA,
G S Gilchrist, and N A Shore
A familial occurrence of osteogenesis imperfecta.
January 1977, The Journal of heredity,
G S Gilchrist, and N A Shore
[Osteogenesis imperfecta. Apropos of a familial case].
October 1985, La Tunisie medicale,
G S Gilchrist, and N A Shore
[Familial cardiomyopathy in osteogenesis imperfecta in children].
December 1986, Pediatriia,
G S Gilchrist, and N A Shore
[Familial cardiomyopathy in osteogenesis imperfecta in children].
January 1987, Pediatriia,
G S Gilchrist, and N A Shore
Osteogenesis imperfecta and osteogenesis imperfecta cystica.
February 1948, The Journal of bone and joint surgery. British volume,
G S Gilchrist, and N A Shore
[Association of osteogenesis imperfecta tarda and familial diabetes mellitus].
March 1974, Der Radiologe,
G S Gilchrist, and N A Shore
Dominant mutations in familial lethal and severe osteogenesis imperfecta.
July 1991, Human genetics,
G S Gilchrist, and N A Shore
Familial occurrence of hyperplastic callus in osteogenesis imperfecta.
January 1997, Archives of orthopaedic and trauma surgery,
G S Gilchrist, and N A Shore
Familial tarda type osteogenesis imperfecta with dentinogenesis imperfecta Type I. Case report.
June 1997, Australian dental journal,
Copied contents to your clipboard!