Genetic counseling in families with spinal muscular atrophy type Kugelberg-Welander
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00285033.pdf
Reference5 articles.
1. Becker PE (1964) Atrophia musculorum spinalis pseudomyopathica. Hereditäre neurogene proximale Amyotrophie von Kugelberg und Welander. Z Menschl Vererb-Konstit Lehre 37:193?220
2. Pauli RM, Motulsky AG (1981) Risk counselling in autosomal dominant disorders with undetermined penetrance. J Med Genet 18:340?343
3. Pearn J (1978) Incidence, prevalence, and gene-frequency studies of chronic childhood spinal muscular atrophy. J Med Genet 15:409?413
4. White NR, Blaw ME (1971) An unusual inheritance pattern for spinal muscular atrophy. Devl med Child Neurol 13:621?624
5. Zellweger H, Schneider H, Schuldt DR (1969) A new genetic variant of spinal muscular atrophy. Neurology 19:865?869
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