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pro vyhledávání: '"Sheila Berggreen"'
Publikováno v:
European Journal of Pediatrics. 136:211-216
A case of deletion of the short arm of chromosome 3 (46,XY,del(3)(p253) is described. The patient is a youth of 18 years in an institution for the mentally retarded. Phenotypically, he presents congenital heart disease, hypertelorism, ptosis, epicant
Publikováno v:
Journal of mental deficiency research. 17(3)
Autor:
Sheila Berggreen
Publikováno v:
BMJ. 283:1612-1612