Clinical and Chromosome Studies of Three Patients with Smith-Magenis Syndrome

Author:

Andel J. F. de Rijk-van,Catsman-Berrevoets C. E.,Hemel J. O.,Hamers A. J. H.

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Inverted neurons in agyria. A Golgi study of a case with abnormal chromosome 17;Bordarier;Human Genetics,1986

2. An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome;Carpenter;Journal of Medical Generics,1981

3. Lissencephaly: diagnosis by computed tomography and magnetic resonance imaging;Cordes;European Journal of Radiology,1988

4. Diagnostic features and clinical signs in 21 patients with lissencephaly;Andel;Developmental Medicine and Child Neurology,1990

5. Miller-Dieker syndrome: lissencephaly and monosomy 17p;Dobyns;Journal of Pediatrics,1983

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1. Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2023-08-16

2. The Spasmodic Upper-body Squeeze: a Chalacteristic Behavior in Smith-Magenis Syndrome;Developmental Medicine & Child Neurology;2008-11-12

3. Abilities and attainment in Smith-Magenis syndrome;Developmental Medicine & Child Neurology;2007-02-13

4. Smith-Magenis Syndrome;Management of Genetic Syndromes;2005-01-14

5. New gene targets related to schizophrenia and other psychiatric disorders: enzymes, binding proteins and transport proteins involved in phospholipid and fatty acid metabolism;Prostaglandins, Leukotrienes and Essential Fatty Acids (PLEFA);1999-03

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