Lucotte G, Berriche S, Fardeau M
Laboratory of Physical Anthropology, Collège de France, Paris.
J Med Genet. 1989 Aug;26(8):485-6. doi: 10.1136/jmg.26.8.485.
Linkage analysis was undertaken in seven French families with facioscapulohumeral muscular dystrophy (FSHD). Six polymorphic DNA probes were studied, including random DNA sequences, coding sequences, and a hypervariable marker. No evidence for linkage of these probes to the disease was detected, and the results exclude probable location of the FSHD gene from three chromosomal regions (16p, proximal 19q, and 21q).
对七个患有面肩肱型肌营养不良症（FSHD）的法国家庭进行了连锁分析。研究了六个多态性DNA探针，包括随机DNA序列、编码序列和一个高变标记。未检测到这些探针与该疾病连锁的证据，结果排除了FSHD基因在三个染色体区域（16p、19q近端和21q）的可能定位。
