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Biomedical Research Institute of New Jersey (BRInj) 140 East Hanover Ave Cedar Knolls New Jersey 07927
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CECAD Institut - University of Cologne Joseph-Stelzmann-Strasse 26 50931 Cologne Germany
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Laboratory of Structural Biology and Cell Signaling Institute of Microbiology of the Czech Acad Sci Prumyslova 595 252 50 Vestec Czech Republic
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Tags
xref:PubMed:33693642
(7)
xref:PubMed:21439053
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xref:PubMed:19304954
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xref:PubMed:42638108
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xref:PubMed:19132335
(1)
xref:PubMed:40461563
(1)
xref:PubMed:30362171
(1)
xref:PubMed:31541176
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Cystic Kidney Disease: Disease Spectrum and Genotype-Phenotype Correlations
Cystic Kidney Disease: Disease Spectrum and Genotype-Phenotype Correlations
PRJNA1274053
|
ENA
Cite
Cystic Kidney Disease: Disease Spectrum and Genotype-Phenotype Correlations
Cystic Kidney Disease: Disease Spectrum and Genotype-Phenotype Correlations
PRJNA1274054
|
ENA
Cite
Genotype-Phenotype Correlations of Late Infantile Neuronal Ceroid Lipofuscinosis - LDN 6716
Genotype-Phenotype Correlations of Late Infantile Neuronal Ceroid Lipofuscinosis - LDN 6716
PRJNA449798
|
ENA
Cite
Genotype-Phenotype Correlations of Late Infantile Neuronal Ceroid Lipofuscinosis - LDN 6716
Genotype-Phenotype Correlations of Late Infantile Neuronal Ceroid Lipofuscinosis - LDN 6716
PRJNA449799
|
ENA
Cite
Genotype-Phenotype Correlations in Angelman Syndrome.
Not available
S-EPMC8304328
|
biostudies-literature
Cite
Genotype-Phenotype Correlations in Children with HHT.
Not available
S-EPMC7565052
|
biostudies-literature
Cite
Unravelling Stargardt Disease (STGD1): Modelling Genotype-Phenotype Correlations and Unresolved Genetic Variants in iPSC-Derived Retinal Organoids
Unravelling Stargardt Disease (STGD1): Modelling Genotype-Phenotype Correlations and Unresolved Genetic Variants in iPSC-Derived Retinal Organoids
PRJNA988887
|
ENA
Cite
Novel SPEG mutations in congenital myopathies: Genotype-phenotype correlations.
Not available
S-EPMC7288247
|
biostudies-literature
Cite
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.
Not available
S-EPMC5777934
|
biostudies-literature
Cite
Intermediate Phenotypes of ATP1A3 Mutations: Phenotype-Genotype Correlations.
Not available
S-EPMC4578012
|
biostudies-literature
Cite
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