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Publications by Rolf Steinmüller
MEHMO (Mental Retardation, Epileptic Seizures, Hypogonadism and -Genitalism, Microcephaly, Obesity), a Novel Syndrome: Assignment of Disease Locus to Xp21.1–p22.13
European Journal of Human Genetics
Genetics
Related publications
MEHMO, a Novel Syndrome: Assignment of Disease Locus to Xp21.1–p22.13
European Journal of Human Genetics
Genetics
Microcephaly, Mental Retardation, Cataracts, and Hypogonadism in Sibs: Martsolf's Syndrome.
Journal of Medical Genetics
Genetics
Defective DNA Polymerase Α-Primase Leads to X-Linked Intellectual Disability Associated With Severe Growth Retardation, Microcephaly, and Hypogonadism
American Journal of Human Genetics
Genetics
Homicide, Fragile X Syndrome, and Mental Retardation
Revista Brasileira de Psiquiatria
Psychiatry
Mental Health
A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34
American Journal of Human Genetics
Genetics
Mosaic Terminal Del(19)(q13.33:) in a Girl With Seizures and Mental Retardation
Journal of Medical Genetics
Genetics
A Systems-Level Approach to Human Epileptic Seizures
Neuroinformatics
Neuroscience
Information Systems
Software
New Onset of Epileptic Seizures Induced by Fahr's Syndrome Secondary to Idiopatic Hypoparathyroidism
Endocrine Abstracts
Androgen Insensitivity With Mental Retardation: A Contiguous Gene Syndrome?
Journal of Medical Genetics
Genetics
