Developmental anomalies of the scapula - The "omo"st forgotten bone

American Journal of Medical Genetics

Volumn 120 A, Issue 4, 2003, Pages 583-587

  Williams, Marc S ^a  

^a GUNDERSEN LUTHERAN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL MODEL; BONE DEFORMATION; BONE DEVELOPMENT; BONE MALFORMATION; CHICK EMBRYO; CONGENITAL MALFORMATION; EMBRYO; EMX2 GENE; GENE; HEMIVERTEBRA; HOMEOBOX; HOXC6 GENE; HUMAN; KLIPPEL FEIL SYNDROME; KOSENOW SYNDROME; LIMB DEVELOPMENT; NONHUMAN; OMOVERTEBRAL BONE; PAX1 GENE; PRIORITY JOURNAL; REVIEW; SCAPULA; SCOLIOSIS; SPINA BIFIDA; SPRENGEL DEFORMITY; SYNDROME DELINEATION; VERTEBRA BODY;

ABNORMALITIES, MULTIPLE; ANIMALS; BONE AND BONES; CHICKENS; DNA-BINDING PROTEINS; FEMALE; HOMEODOMAIN PROTEINS; HUMANS; MICE; PAIRED BOX TRANSCRIPTION FACTORS; PREGNANCY; SCAPULA; TRANSCRIPTION FACTORS; ULTRASONOGRAPHY;

EID: 0041823263     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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