RETESTING FOR FRAGILE X SYNDROME IN CYTOGENETICALLY NORMAL MALES
Saved in:
GRINGRAS, P., BARNICOAT, A., RETESTING FOR FRAGILE X SYNDROME IN CYTOGENETICALLY NORMAL MALES. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, Vol. 40, no. 1 (1998), p. 62-64.
Ref.
67774
Location:
SIIS R.727
Palabras clave:
Cromosoma X, Diagnóstico, Discapacidad intelectual, Evaluación, Instrumentos técnicos
Cromosoma X, Diagnóstico, Discapacidad intelectual, Evaluación, Instrumentos técnicos
Be the first to leave a comment!