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Results of search for 'au:"Vallandro, C"'
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Authors
Azambuja, N A
Brizolara, A
Brodtmann, B
Mendez, H M
Paskulin, G A
Rotta, N T
Vallandro, C
Vilgas, J
dos Santos Farias, A
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Abnormalities, Multiple
Adolescent
Biopsy
Cerebellar Ataxia
Cerebral Palsy
Child
Consanguinity
Female
Genes, Recessive
Humans
Intellectual Disability
Male
Microcephaly
Muscular Dystrophies
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complications
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1.
The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients.
[electronic resource]
by
Mendez, H M
Paskulin, G A
Vallandro, C
Producer:
19851118
In:
American journal of medical genetics
vol. 22
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Available from publisher's website
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2.
[Association of myopathy with ataxia and pyramidalism. Study of 2 brothers].
[electronic resource]
by
Rotta, N T
Brizolara, A
Vallandro, C
dos Santos Farias, A
Azambuja, N A
Brodtmann, B
Vilgas, J
Producer:
19741219
In:
Arquivos de neuro-psiquiatria
vol. 32
Online resources:
Available from publisher's website
Availability:
No items available.
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