Don't use the term "amyoplasia" loosely [2]

American Journal of Medical Genetics

Volumn 111, Issue 3, 2002, Pages 344-

  Hall, Judith G ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTHROGRYPOSIS; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 2; CHROMOSOME 5; CHROMOSOME INSERTION; DISEASE ASSOCIATION; GENETIC DISORDER; HYDRAMNIOS; LETTER; PRIORITY JOURNAL; CLASSIFICATION; HUMAN; NOMENCLATURE; NOTE;

ARTHROGRYPOSIS; HUMAN; TERMINOLOGY; HUMANS;

INSERTION SEQUENCES;

EID: 0037102941     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10571     Document Type: Letter

References (6)

1. Amyoplasia associated with a balanced de novo insertion of a segment of the long arm of chromosome 5 into chromosome 2
2. A dominantly inherited lower motor neuron disorder presenting at birth with associated arthrogryposis
3. Part I. Amyoplasie: A common, sporadic condition with congenital contractures
4. Pelvic dysplasia associated with arthrogrypotic changes in the lower extremities. A new syndrome
5. Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: A distinct autosomal-recessive disorder
6. Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosome