Abnormal clavicles in a neonate with partial monosomy 21

Pediatric Radiology

Volumn 29, Issue 3, 1999, Pages 221-222

  Wang, Sharon H ^a   Aftimos, Salim ^a  

^a NATIONAL WOMEN S HOSPITAL   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BONE MALFORMATION; CASE REPORT; CHROMOSOME 21; CLAVICLE; CLINICAL FEATURE; HUMAN; MALE; NEWBORN; PARTIAL MONOSOMY; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 21; CLAVICLE; DIAGNOSIS, DIFFERENTIAL; HUMANS; INFANT, NEWBORN; MALE; PHENOTYPE;

EID: 0032981561     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002470050576     Document Type: Article

References (5)

1. Taybi H, Lachman RS (1996) Radiology of syndromes, metabolic disorders and skeletal dysplasias, 4th edn. Mosby, St. Louis, pp 1048-1049
2. Bamforth JS, Leonard CO, Chodirker BN, et al (1989) Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome. Am J Med Genet 32: 93-99
3. Richer L, Fitch N, Sitahal S, et al (1981) Analysis of banding patterns in a case of ring chromosome 21. Am J Med Genet 10: 323-331
4. Chettouh Z, Croquette MF. Delobel B, et al (1995) Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region. Am J Hum Genet 57: 62-71
5. Shibata K, Waldenmaier C, Hirsch W (1973) A child with a 21-ring chromosome 45,XX,21-/46,XX,2/r investigated with the banding technique. Human-genetik 18: 315-319