A case of Roberts syndrome described in 1737 [10]

Journal of Medical Genetics

Volumn 38, Issue 8, 2001, Pages 565-567

  Bates, A W ^a  

^a ROYAL LONDON HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME ABERRATION; ENCEPHALOCELE; HUMAN; LETTER; PRIORITY JOURNAL; ROBERTS SYNDROME; STILLBIRTH;

ABNORMALITIES, MULTIPLE; CRANIOFACIAL ABNORMALITIES; ECTROMELIA; ENCEPHALOCELE; FETAL DEATH; GENES, RECESSIVE; HISTORY, 18TH CENTURY; HUMANS; INFANT, NEWBORN; MALE; SYNDROME;

EID: 0034885038     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (12)

1. Roberts syndrome: A review of 100 cases and a new rating system for severity
2. The Roberts syndrome
3. Roberts syndrome: Phenotypic variation, cytogenetic definition and heterozygote detection
4. Roberts syndrome: Clinical and cytogenetic aspects
5. Bartsocas-Papas syndrome with internal anomalies: Evidence for a more generalized epithelial defect or new syndrome?
6. Nager acrofacial dysostosis
7. The SC phocomelia syndrome: Report of two cases with cytogenetic abnormality
8. A child with double cleft lip and palate, protrusion of the intermaxillary portion of the upper jaw and imperfect development of the bones of the four extremities
9. Tetraphocomelia and bilateral cleft lip in a historical case of Roberts syndrome (Virchow, 1898)
10. Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. I. Syndromes with multiple congenital abnormalities
11. Infante monstroso Lugduni in viam publicam die V. Martii A. MDCLXXI. exposito