PubMed (OMIM) for id: 375855

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Year	Number of Results
1989	1
1994	1
1998	2
1999	1
2002	1
2023	0

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MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder.

Leshinsky-Silver E, Zinger A, Bibi CN, Barash V, Sadeh M, Lev D, Sagie TL. Leshinsky-Silver E, et al. Eur J Hum Genet. 2002 Apr;10(4):226-30. doi: 10.1038/sj.ejhg.5200791. Eur J Hum Genet. 2002. PMID: 12032729

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

DeLozier-Blanchet CD, Haenggeli CA, Bottani A. DeLozier-Blanchet CD, et al. Eur J Hum Genet. 1999 Sep;7(6):621-2. doi: 10.1038/sj.ejhg.5200364. Eur J Hum Genet. 1999. PMID: 10482947 No abstract available.

MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to xp21.1-p22.13.

Steinmüller R, Steinberger D, Müller U. Steinmüller R, et al. Eur J Hum Genet. 1998 May-Jun;6(3):201-6. doi: 10.1038/sj.ejhg.5200180. Eur J Hum Genet. 1998. PMID: 9781023

Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution.

Ehrmann IE, Ellis PS, Mazeyrat S, Duthie S, Brockdorff N, Mattei MG, Gavin MA, Affara NA, Brown GM, Simpson E, Mitchell MJ, Scott DM. Ehrmann IE, et al. Hum Mol Genet. 1998 Oct;7(11):1725-37. doi: 10.1093/hmg/7.11.1725. Hum Mol Genet. 1998. PMID: 9736774

Translation initiation factor eIF-2. Cloning and expression of the human cDNA encoding the gamma-subunit.

Gaspar NJ, Kinzy TG, Scherer BJ, Hümbelin M, Hershey JW, Merrick WC. Gaspar NJ, et al. J Biol Chem. 1994 Feb 4;269(5):3415-22. J Biol Chem. 1994. PMID: 8106381 Free article.

[Microencephalic nanism, severe retardation, hypertonia, obesity, and hypogonadism in two brothers: a new syndrome?].

Delozier-Blanchet CD, Haenggeli CA, Engel E. Delozier-Blanchet CD, et al. J Genet Hum. 1989 Dec;37(4-5):353-65. J Genet Hum. 1989. PMID: 2635712 French.

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