INFANTS AND CHILDREN WITH HEARING LOSS: PART I
Tallennettuna:
VARIOS AUTORES, INFANTS AND CHILDREN WITH HEARING LOSS: PART I. MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, Vol. 9, no. 2 (2003), p. 61-131.
Ref.
122673
Sijainti:
SIIS R.1376
Palabras clave:
Detección, Discapacidad auditiva, Etiología, Genética, Infancia, Tratamiento médico
Detección, Discapacidad auditiva, Etiología, Genética, Infancia, Tratamiento médico
Abstrakti:
Traducción en castellano: Revista Síndrome de Down, 20(2), 77, 2003, pp. 63-76.
Traducción en castellano: Revista Síndrome de Down, 20(2), 77, 2003, pp. 63-76.
Samankaltaisia teoksia: INFANTS AND CHILDREN WITH HEARING LOSS: PART I
- INFANTS AND CHILDREN WITH HEARING LOSS: PART II
- SCREENING INFANTS FOR HEARING LOSS
- Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss
- SCREENING PROCEDURES USED TO IDENTIFY CHILDREN WITH HEARING LOSS
- CANONICAL SYLLABLE REDUPLICATION AND VARIEGATION IN INFANTS WITH SENSORINEURAL HEARING LOSS
- COMMUNICATION BEHAVIORS OF INFANTS WITH HEARING LOSS AND THEIR HEARING MOTHERS