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N Feingold

机构:Inserm, Hôpital Saint-Louis

发表论文 101 篇 · 总被引 1890 次 · h-index 22

代表论文

  • Juvenile limb-girdle muscular dystrophy (1996 · Brain · 被引 201)
  • Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping (1994 · Human Molecular Genetics · 被引 199)
  • A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. (1991 · PubMed · 被引 156)
  • Phaeochromocytoma in multiple endocrine neoplasia type 2 A: survey of 100 cases (1993 · Clinical Endocrinology · 被引 98)
  • Genetic markers in chronic air-flow limitation. A genetic epidemiologic study. (1983 · PubMed · 被引 57)
  • Keratoderma with scleroatrophy of the extremities or sclerotylosis (Huriez syndrome): a reappraisal (1995 · British Journal of Dermatology · 被引 50)