Literature DB >> 5119919

An unusual inheritane pattern for spinal muscular atrophy.

N R White, M E Blaw.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5119919     DOI： 10.1111/j.1469-8749.1971.tb08326.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN： 0012-1622            Impact factor:   5.449


× No keyword cloud information.
  3 in total

1.  Anterior horn cell disease associated with pontocerebellar hypoplasia in infants.

Authors:  F Goutières; J Aicardi; E Farkas
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-04       Impact factor: 10.154

2.  A new genetic variant of the spinal muscular atrophies in infancy.

Authors:  H Zellweger; E Hanhart; H J Schneider
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

3.  Genetic counseling in families with spinal muscular atrophy type Kugelberg-Welander.

Authors:  K Zerres; T Grimm
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.