共 50 条
- [42] Amyoplasia congenita (arthrogryposis multiplex congenita) JOURNAL OF PEDIATRICS, 1939, 15 : 551 - 557
- [44] Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly Human Genetics, 2023, 142 : 543 - 552
- [46] Arthrogryposis multiplex congenita and retinitis pigmentosa [Arthrogryposis multiplex congenita und Retinitis pigmentosa] Der Ophthalmologe, 2009, 106 (12): : 1121 - 1125
- [47] MYOTONIA CONGENITA WITH AUTOSOMAL DOMINANT OR RECESSIVE INHERITANCE - 16 CASES SEMAINE DES HOPITAUX, 1989, 65 (34): : 2093 - 2098
- [49] ARTHROGRYPOSIS MULTIPLEX CONGENITAL MYOPATHIC TYPE ISRAEL JOURNAL OF MEDICAL SCIENCES, 1973, 9 (04): : 463 - 468