HOMOCYSTINURIA. CLINICAL, BIOCHEMICAL AND GENETIC ASPECTS OF CYSTATHIONINE B-SYNTHASE AND ITS DEFICIENCY IN MAN
Kaydedildi:
SKOVBY, F., HOMOCYSTINURIA. CLINICAL, BIOCHEMICAL AND GENETIC ASPECTS OF CYSTATHIONINE B-SYNTHASE AND ITS DEFICIENCY IN MAN. ACTA PAEDIATRICA SCANDINAVICA, no. SUPLEMENTO 321 (1985), p. 21.
Ref.
5132
Yer:
SIIS R.386 Depósito (26/29/30)
Palabras clave:
Diagnóstico prenatal, Metabolopatías, Tratamiento
Diagnóstico prenatal, Metabolopatías, Tratamiento
Benzer Materyaller: HOMOCYSTINURIA. CLINICAL, BIOCHEMICAL AND GENETIC ASPECTS OF CYSTATHIONINE B-SYNTHASE AND ITS DEFICIENCY IN MAN
- PRENATAL DIAGNOSIS OF DYSMORPHIC NEONATAL-LETHAL TYPE II GLUTARICACIDURIA
- CLINICAL AND BIOCHEMICAL APPROACH TO THE NEONATE WITH A SUSPECTED INBORN ERROR OF AMINO ACID AND ORGANIC ACID METABOLISM
- EXPERIENCIA EN EL DIAGNOSTICO PRENATAL DE 45 CASOS DE AMINOACIDOPATIAS Y ACIDEMIAS ORGANICAS
- POSSIBILITIES FOR TREATMENT AND FOR EARLY PRENATAL DIAGNOSIS OF HEREDITARY TYROSINAEMIA
- THE UNBORN PATIENT. PRENATAL DIAGNOSIS AND TREATMENT
- THE EMOTIONAL IMPLICATIONS OF PRENATAL DIAGNOSIS. EN:PSYCHOLOGICAL ASPECTS OF GENETIC COUNSELLING