TY  - GEN
AU  - Poznanski,A K
AU  - Stern,A M
AU  - Gall,J C
TI  - Skeletal anomalies in genetically determined congenital heart disease
SN  - 0033-8389
PY  - 1972///0619
KW  - Abnormalities, Multiple
KW  - diagnostic imaging
KW  - Adolescent
KW  - Adult
KW  - Arm
KW  - abnormalities
KW  - Body Constitution
KW  - Bone Diseases
KW  - Bone Diseases, Developmental
KW  - complications
KW  - Bone and Bones
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Aberrations
KW  - Chromosome Disorders
KW  - Cleft Palate
KW  - Craniosynostoses
KW  - Ellis-Van Creveld Syndrome
KW  - Face
KW  - Female
KW  - Fingers
KW  - Heart Defects, Congenital
KW  - Humans
KW  - Hypercalcemia
KW  - Hypogonadism
KW  - Infant
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - Klippel-Feil Syndrome
KW  - Laurence-Moon Syndrome
KW  - Lentigo
KW  - Male
KW  - Marfan Syndrome
KW  - Obesity
KW  - Pierre Robin Syndrome
KW  - Radiography
KW  - Radius
KW  - Scoliosis
KW  - Thrombocytopenia
KW  - Toes
KW  - Turner Syndrome
N1  - Publication Type: Journal Article
ER  -