Research map: Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly

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  1. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology · Sue M. Richards · 2015 · 33500 citations · Cited by this paper
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  22. Identification of a fourth Nuclear Factor I gene in chicken by cDNA cloning: NFI-X · Ulrich Kruse · 1991 · 73 citations · Cited by this paper
  23. NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly · Ina Schanze · 2018 · 71 citations · Cited by this paper
  24. Variants in nuclear factor I genes influence growth and development · Martin Zenker · 2019 · 57 citations · Cited by this paper
  25. Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes · Francisco Martı́nez · 2015 · 53 citations · Cited by this paper
  26. Combined allelic dosage of Nfia and Nfib regulates cortical development · Jens Bunt · 2017 · 43 citations · Cited by this paper
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  31. Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon‐level Array, and RNA sequencing · Jian Zhao · 2024 · 3 citations · Cited by this paper
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