Barth, P. G.
2589  Ergebnisse:
Personensuche X
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1

Sequential MR Imaging Changes in Nonketotic Hyperglycinemia:

Mourmans, J ; Majoie, C.B.L.M ; Barth, P.G...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7976062/.  , 2006
 
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2

POMT2 mutations cause alpha-dystroglycan hypoglycosylation ..:

van Reeuwijk, J ; Janssen, M.H.M ; van den Elzen, C...
van Reeuwijk , J , Janssen , M H M , van den Elzen , C , de Beltran-Valero Bernabe , D , Sabatelli , P , Merlini , L , Boon , ME , Scheffer , H , Brockington , M , Muntoni , F , Huynen , M , Verrips , A , Walsh , C E , Barth , P G , Brunner , H G & van Bokhoven , H 2005 , ' POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome ' , Journal of Medical Genetics , vol. 42 , no. 12 , pp. 907-12 . https://doi.org/10.1136/jmg.2005.031963.  , 2005
 
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3

X chromosome inactivation in carriers of Barth syndrome:

Orstavik, K H ; Orstavik, R E ; Naumova, A K...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1377557.  , 1998
 
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4

The X-linked gene G4.5 is responsible for different infanti..:

D'Adamo, P ; Fassone, L ; Gedeon, A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1715993.  , 1997
 
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5

Autosomal dominant cerebellar ataxia with retinal degenerat..:

Jöbsis, G J ; Weber, J W ; Barth, P G...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1074093.  , 1997
 
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7

Spectrum of mutations in the gene encoding the adrenoleukod..:

Ligtenberg, M J ; Kemp, S ; Sarde, C O...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1801307.  , 1995
 
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9

Schizencephaly and nonlissencephalic cortical dysplasias:

Barth, P G
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8331722/.  , 1992
 
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