“…Duplication of the distal part of the long arm of chromosome 8 has been reported several times (ABUELO et al 1977;BALLESTA et al 1980;CHITHAM et al 1977;FRYNS et al 1974;LAURENT et al 1974;LEJEUNE and RETHORE 1973;LEJEUNE et al 1972;RETHORE et al 1977; SANCHEZ and YUNIS 1974;SCHINZEL 1977). However, the breakpoints on chromosome 8 have varied between q21 and 924, and no consistent syndrome has yet emerged.…”
A newborn boy with mental retardation, epilepsy, heart malformation and minor somatic abnormalities was found to have a 46, XY,‐13,+der(13), t(8;13) (q21;p11) karyotype. The balanced form of the translocation was observed in the mother.
“…Duplication of the distal part of the long arm of chromosome 8 has been reported several times (ABUELO et al 1977;BALLESTA et al 1980;CHITHAM et al 1977;FRYNS et al 1974;LAURENT et al 1974;LEJEUNE and RETHORE 1973;LEJEUNE et al 1972;RETHORE et al 1977; SANCHEZ and YUNIS 1974;SCHINZEL 1977). However, the breakpoints on chromosome 8 have varied between q21 and 924, and no consistent syndrome has yet emerged.…”
A newborn boy with mental retardation, epilepsy, heart malformation and minor somatic abnormalities was found to have a 46, XY,‐13,+der(13), t(8;13) (q21;p11) karyotype. The balanced form of the translocation was observed in the mother.
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