Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

Proceedings of the National Academy of Sciences of the United States of America

Volumn 86, Issue 24, 1989, Pages 10001-10005

  Ballabio, A ^a   Bardoni, B ^a   Carrozzo, R ^a   Andria, G ^a   Bick, D ^a   Campbell, L ^a   Hamel, B ^a   Ferguson Smith, M A ^a   Gimelli, G ^a   Fraccaro, M ^a   Maraschio, P ^a   Zuffardi, O ^a   Guioli, S ^a   Camerino, G ^a  

^a UNIVERSITY MEDITERRANEA OF REGGIO CALABRIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHONDRODYSPLASIA PUNCTATA; CHROMOSOME XP; CLINICAL ARTICLE; GENE DELETION; HEREDITY; HUMAN; KALLMANN SYNDROME; MENTAL DEFICIENCY; PRIORITY JOURNAL; SHORT STATURE; STERYL SULFATASE DEFICIENCY; X CHROMOSOMAL INHERITANCE;

CHROMOSOME DELETION; CHROMOSOME MAPPING; DNA; FEMALE; HUMAN; KARYOTYPING; MALE; MENTAL RETARDATION; SEX CHROMOSOME ABERRATIONS; SUPPORT, NON-U.S. GOV'T; SYNDROME; TRANSLOCATION (GENETICS); X CHROMOSOME; Y CHROMOSOME;

EID: 0024802646     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.86.24.10001     Document Type: Article

References (0)