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Insertion Of The Il1rapl1 Gene Into The Duplication Junction Of The Dystrophin Gene Journal Of Human Genetics
New Variants Challenges And Pitfalls In Dmd Genotyping Implications In Diagnosis Prognosis And Therapy Journal Of Human Genetics
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Gonadal Mosaicism Of A Novel Iqsec2 Variant Causing Female Limited Intellectual Disability And Epilepsy European Journal Of Human Genetics
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Genetic Effects Have A Dominant Role On Poor Responses To Infant Vaccination To Hepatitis B Virus Journal Of Human Genetics
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Genotype Instability During Long Term Subculture Of Lymphoblastoid Cell Lines Journal Of Human Genetics
Important And Critical Scientific Aspects In Pharmacogenomics Analysis Lessons From Controversial Results Of Tamoxifen And Cyp2d6 Studies Journal Of Human Genetics
Common Variants Of Slamf1 And Itln1 On 1q21 Are Associated With Type 2 Diabetes In Indian Population Journal Of Human Genetics
A Splicing Mutation Of The Hmga2 Gene Is Associated With Silver Russell Syndrome Phenotype Journal Of Human Genetics
Serotonin 1a Receptor Gene And Major Depressive Disorder An Association Study And Meta Analysis Journal Of Human Genetics
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Deciphering Transcription Dysregulation In Fsh Muscular Dystrophy Journal Of Human Genetics
Contribution Of Common And Rare Variants Of The Ptchd1 Gene To Autism Spectrum Disorders And Intellectual Disability European Journal Of Human Genetics
Functional And Genetic Diversity Of Leukocyte Immunoglobulin Like Receptor And Implication For Disease Associations Journal Of Human Genetics
Association Of Tmem18 Variants With Bmi And Waist Circumference In Children And Correlation Of Mrna Expression In The Pfc With Body Weight In Rats European Journal Of Human Genetics
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Late Onset Episodic Ataxia Associated With Slc1a3 Mutation Journal Of Human Genetics
Identification Of Functional Nucleotide And Haplotype Variants In The Promoter Of The Cebpe Gene Journal Of Human Genetics
