DE NOVO FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY DEFINED BY DNA PROBE P13E (D4F104S1)
Kaydedildi:
JARDINE, P.E., ET AL., DE NOVO FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY DEFINED BY DNA PROBE P13E (D4F104S1). ARCHIVES OF DISEASE IN CHILDHOOD, Vol. 71, no. 3 (1994), p. 221-227.
Ref.
40563
Yer:
SIIS R.186
Palabras clave:
Casuística, Discapacidad, Discapacidad física y orgánica, Discapacidad sensorial, Distrofia muscular
Casuística, Discapacidad, Discapacidad física y orgánica, Discapacidad sensorial, Distrofia muscular
Benzer Materyaller: DE NOVO FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY DEFINED BY DNA PROBE P13E (D4F104S1)
- PRENATAL DIAGNOSIS USING DNA PROBES IN TWINS AT RISK FOR DUCHENNE MUSCULAR DISTROPHY
- SCREENING FOR DUCHENNE MUSCULAR DYSTROPHY
- GENETICS AND THE MUSCULAR DYSTROPHIES
- USEFULNESS OF TEST: MANUAL MUSCLE TESTING, GONIOMETRY, AND DAILY ACTIVITIES FOR DIFFERENTIAL DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY, BECKER'S MILD MUSCULAR DYSTROPHY AND BECKER'S SEVERE MUSCULAR DYSTROPHY
- INHERITANCE AND THE MUSCULAR DYSTROPHIES
- PARENTS' PERSPECTIVES ON COPING WITH DUCHENNE MUSCULAR DYSTROPHY