Endochondral ossification in achondroplastic dwarfism. 1970

D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg

UI MeSH Term Description Entries
D007085 Ilium The largest of three bones that make up each half of the pelvic girdle. Auricular Surface of Ilium,Iliac Crest,Iliac Crest Bone,Iliac Fossa,Bones, Iliac Crest,Crest Bone, Iliac,Crest Bones, Iliac,Crest, Iliac,Crests, Iliac,Fossa, Iliac,Iliac Crest Bones,Iliac Crests,Iliums
D007223 Infant A child between 1 and 23 months of age. Infants
D008297 Male Males
D009999 Ossification, Heterotopic The development of bony substance in normally soft structures. Ossification, Pathologic,Ectopic Ossification,Heterotopic Ossification,Ossification, Ectopic,Ossification, Pathological,Pathologic Ossification,Pathological Ossification
D011859 Radiography Examination of any part of the body for diagnostic purposes by means of X-RAYS or GAMMA RAYS, recording the image on a sensitized surface (such as photographic film). Radiology, Diagnostic X-Ray,Roentgenography,X-Ray, Diagnostic,Diagnostic X-Ray,Diagnostic X-Ray Radiology,X-Ray Radiology, Diagnostic,Diagnostic X Ray,Diagnostic X Ray Radiology,Diagnostic X-Rays,Radiology, Diagnostic X Ray,X Ray Radiology, Diagnostic,X Ray, Diagnostic,X-Rays, Diagnostic
D002356 Cartilage A non-vascular form of connective tissue composed of CHONDROCYTES embedded in a matrix that includes CHONDROITIN SULFATE and various types of FIBRILLAR COLLAGEN. There are three major types: HYALINE CARTILAGE; FIBROCARTILAGE; and ELASTIC CARTILAGE. Cartilages
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D002806 Chondrodysplasia Punctata A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC), an autosomal dominant form (Conradi-Hunermann syndrome), and a milder X-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form. Chondrodystrophia Calcificans Congenita,Conradi-Hunermann Syndrome,Dysplasia Epiphysialis Punctata,Epiphyses, Stippled,Stippled Epiphyses,Chondrodysplasia Punctata 2, X-Linked,Chondrodysplasia Punctata 2, X-Linked Dominant,Conradi Hunermann Happle Syndrome,Conradi-Hunermann-Happle Syndrome,Conradi-Hünermann Syndrome,Conradi-Hünermann-Happle Syndrome,Happle Syndrome,Hunermann-Conradi Syndrome,X-Linked Chondrodysplasia Punctata 2,X-Linked Dominant Chondrodysplasia Punctata,Chondrodysplasia Punctata 2, X Linked,Chondrodysplasia Punctata 2, X Linked Dominant,Conradi Hunermann Syndrome,Conradi Hünermann Happle Syndrome,Conradi Hünermann Syndrome,Conradi-Hunermann-Happle Syndromes,Conradi-Hünermann Syndromes,Conradi-Hünermann-Happle Syndromes,Hunermann Conradi Syndrome,X Linked Chondrodysplasia Punctata 2,X Linked Dominant Chondrodysplasia Punctata
D004392 Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. Nanism

Related Publications

D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
January 1976, Annales Academiae Medicae Stetinensis,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
January 1976, Clinical orthopaedics and related research,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
January 1970, Revue de laryngologie - otologie - rhinologie,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
March 1974, Veterinary medicine, small animal clinician : VM, SAC,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
February 1980, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
January 1975, Birth defects original article series,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
January 1974, Chronobiologia,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
December 2007, The journal of gene medicine,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
August 2000, Journal of theoretical biology,
D L Rimoin, and G N Hughes, and R L Kaufman, and R E Rosenthal, and W H McAlister, and R Silberberg
June 2016, Journal of developmental biology,
Copied contents to your clipboard!