The continuing failure to recognise Alstrom syndrome and further evidence of genetic homogeneity

Journal of Medical Genetics

Volumn 37, Issue 3, 2000, Pages 219-

  Deeble, V J ^a   Roberts, E ^a   Jackson, A ^a   Lench, N ^a   Karbani, G ^a   Woods, C G ^a  

^a ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALSTROM SYNDROME; BARDET BIEDL SYNDROME; CARDIOMYOPATHY; CHROMOSOME 2P; CONGENITAL BLINDNESS; CONGENITAL DEAFNESS; CONGENITAL NYSTAGMUS; DIABETES MELLITUS; DIAGNOSTIC ERROR; DISORDERS OF MITOCHONDRIAL FUNCTIONS; HEART DILATATION; HUMAN; LEBER CONGENITAL AMAUROSIS; LETTER; OBESITY; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; USHER SYNDROME;

ADULT; CARDIOMYOPATHY, DILATED; DEAFNESS; DIAGNOSTIC ERRORS; EYE DISEASES, HEREDITARY; FEMALE; GENETIC HETEROGENEITY; HUMANS; MALE; OBESITY; PEDIGREE; SYNDROME; VISION DISORDERS;

EID: 0034111554     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (6)