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English

MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity

Published inEuropean journal of human genetics, vol. 7, no. 6, p. 621-622
Publication date1999
Keywords
  • Abnormalities, Multiple
  • Adolescent
  • Child, Preschool
  • Chromosome Mapping
  • Diagnosis, Differential
  • Electroencephalography
  • Epilepsy/genetics
  • Genetic Linkage
  • Humans
  • Hypogonadism/genetics
  • Infant
  • Intellectual Disability/genetics
  • Male
  • Microcephaly/genetics
  • Obesity/genetics
  • Syndrome
  • X Chromosome
Citation (ISO format)
DELOZIER-BLANCHET, C, HAENGGELI, Charles-Antoine, BOTTANI, Armand. MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity. In: European journal of human genetics, 1999, vol. 7, n° 6, p. 621–622. doi: 10.1038/sj.ejhg.5200364
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Article (Published version)
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Identifiers
ISSN of the journal1018-4813
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