MEHMO, a novel syndrome: Assignment of disease locus to Xp21.1-p22.13 [1]

European Journal of Human Genetics

Volumn 7, Issue 6, 1999, Pages 621-622

  Delozier Blanchet, Célia D ^a   Haenggeli, Charles Antoine ^a   Bottani, Armand ^a  

^a GENEVA UNIVERSITY HOSPITALS   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME DISORDER; CHROMOSOME XP; DEVELOPMENTAL DISORDER; DIFFERENTIAL DIAGNOSIS; FACE DEFORMITY; GENETIC LINKAGE; GROWTH RETARDATION; HUMAN; HYPOGONADISM; LETTER; MALE; MENTAL DEFICIENCY; MICROCEPHALY; MUSCLE HYPERTONIA; OBESITY; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD, PRESCHOOL; CHROMOSOME MAPPING; DIAGNOSIS, DIFFERENTIAL; ELECTROENCEPHALOGRAPHY; EPILEPSY; HUMANS; HYPOGONADISM; INFANT; LINKAGE (GENETICS); MALE; MENTAL RETARDATION; MICROCEPHALY; OBESITY; SYNDROME; X CHROMOSOME;

EID: 0032848013     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200364     Document Type: Letter

References (3)

1. Steinmüller R, Steinberger D, Müller U: MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to Xp21.2-p22.13. Eur J Hum Genet 1998; 6: 201-206.
2. DeLozier-Blanchet CD, Haenggeli CA, Engel E: Nanisme microcéphalique, arriération sévère, hypertonie, obésité et hypogénitalisme chez deux frères: Un nouveau syndrome? J Génét Hum 1989; 37: 353-365.
3. Winter RM, Baraitser M: London Dysmorphology Database. Oxford Medical Databases, Oxford University Press. 1996.