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As a result of this case report, several entities are postulated due to an extra metacentric D or E chromosome: 1) infants presenting with a phenotype similar to the E 18 trisomy; however, the karyotype can be interpreted as either a deleted E or D chromosome; 2) another group of children all presenting with mental retardation, facial asymmetry, scoliosis and cerebral palsy, postulated due to a partial trisomy of E 16 or E 17; 3) individuals with a normal phenotype, but chromosomally presented with an additional satellited metacentric chromosome consistent with centric fusion of a D or G chromosome and 4) children presenting with an inconsistent phenotype and chromosomally presenting with an extra chromosome manifesting satellites or satellite association; the same chromosome abnormality often is found in unaffected parents and/or sibs.
K W Dumars, and
G Fialko, and
E Larson
March 1979,
Journal de genetique humaine,
K W Dumars, and
G Fialko, and
E Larson
September 1970,
Annales de genetique,
K W Dumars, and
G Fialko, and
E Larson
November 1975,
Clinical genetics,
K W Dumars, and
G Fialko, and
E Larson
December 1978,
Journal de genetique humaine,
K W Dumars, and
G Fialko, and
E Larson
January 1973,
Hereditas,
K W Dumars, and
G Fialko, and
E Larson
January 1971,
Annales de pediatrie,
K W Dumars, and
G Fialko, and
E Larson
July 1966,
Folia hereditaria et pathologica,
K W Dumars, and
G Fialko, and
E Larson
December 1963,
Lancet (London, England),
K W Dumars, and
G Fialko, and
E Larson
July 1979,
Clinical genetics,
K W Dumars, and
G Fialko, and
E Larson
March 1986,
Clinical genetics,
