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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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 Haenggeli, Charles-Antoine Bottani, Armand
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		DOI: 10.1038/sj.ejhg.5200364 PMID: 10482947
Full text		Article (Published version) (134 Kb) - Free access
Structures		Faculté de médecine / Section de médecine fondamentale / Département de médecine génétique et développement Faculté de médecine / Section de médecine clinique / Département de pédiatrie, gynécologie et obstétrique
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

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