A POPULATION STUDY OF CHROMOSOME 22q11 DELETIONS IN INFANCY
Saved in:
GOODSHIP, J., ET AL., A POPULATION STUDY OF CHROMOSOME 22q11 DELETIONS IN INFANCY. ARCHIVES OF DISEASE IN CHILDHOOD, Vol. 79, no. 4 (1998), p. 348-351.
Ref.
76561
Location:
SIIS R.186 Archivo
Palabras clave:
Anomalías cromosómicas, Datos epidemiológicos, Discapacidad, Síndromes, Reino Unido
Anomalías cromosómicas, Datos epidemiológicos, Discapacidad, Síndromes, Reino Unido
Similar Items: A POPULATION STUDY OF CHROMOSOME 22q11 DELETIONS IN INFANCY
- Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions
- Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome
- TOWARDS EARLIER DIAGNOSIS OF 22q11 DELETIONS
- AUTISM, ADHD, MENTAL RETARDATION AND BEHAVIOR PROBLEMS IN 100 INDIVIDUALS WITH 22Q11 DELETION SYNDROME
- UNBALANCED FORM OF TRANSLOCATION DELETION BETWEEN CHROMOSOMES 6 AND 22 IN A MENTALLY HANDICAPPED FEMALE [45,XX,-6,-22,+DER(6),T(6 / 22)(Q25.1:Q11.2)]
- Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome