DERMATOGLYPHIC ANALYSES OF 32 PARENTS OF PRADER-WILLI SYNDROME INDIVIDUALS
محفوظ في:
SMITH, A., SIMPSON, E., DERMATOGLYPHIC ANALYSES OF 32 PARENTS OF PRADER-WILLI SYNDROME INDIVIDUALS. JOURNAL OF MENTAL DEFICIENCY RESEARCH, Vol. 28, no. 4 (1984), p. 275-280.
Ref.
4114
الموقع:
SIIS R.104 Depósito (5)
Palabras clave:
Dermatoglifos, Genética, Investigación, Síndrome de Prader-Willi
Dermatoglifos, Genética, Investigación, Síndrome de Prader-Willi
مواد مشابهة: DERMATOGLYPHIC ANALYSES OF 32 PARENTS OF PRADER-WILLI SYNDROME INDIVIDUALS
- CHROMOSOME FINDINGS IN THE PRADER-WILLI SYNDROME
- DIAGNOSIS IN PRADER-WILLI SYNDROME
- PRADER-WILLI SYNDROME: AN OVERVIEW
- PRADER WILLI SYNDROME WITH HYPOTHYROIDISM
- USING STABLE ISOTOPES TO ASSESS REDUCED PHYSICAL ACTIVITY OF INDIVIDUALS WITH PRADER-WILLI SYNDROME
- NALTREXONE AND FLUOXETINE IN PRADER-WILLI SYNDROME