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Title

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

Authors
DeLozier-Blanchet, C
Published in European Journal of Human Genetics. 1999, vol. 7, no. 6, p. 621-2
Keywords Abnormalities, MultipleAdolescentChild, PreschoolChromosome MappingDiagnosis, DifferentialElectroencephalographyEpilepsy/geneticsGenetic LinkageHumansHypogonadism/geneticsInfantIntellectual Disability/geneticsMaleMicrocephaly/geneticsObesity/geneticsSyndromeX Chromosome
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PMID: 10482947
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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. 621-2. https://archive-ouverte.unige.ch/unige:74316

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Deposited on : 2015-07-27

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