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MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity |
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Published in | European Journal of Human Genetics. 1999, vol. 7, no. 6, p. 621-2 | |
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 | |
Identifiers | PMID: 10482947 | |
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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. 621-2. doi: 10.1038/sj.ejhg.5200364 https://archive-ouverte.unige.ch/unige:74316 |