T. Parker

发表

Autosomal dominant polycystic kidney disease caused by somatic and germline mosaicism

H. Rennert, J. Blumenfeld, A. Tan, 2015, Clinical genetics.

A common intronic single nucleotide variant modifies PKD1 expression level

H. Rennert, I. Barash, Pengbo Zhou, 2022, Clinical genetics.

Development and validation of a whole genome amplification long-range PCR sequencing method for ADPKD genotyping of low-level DNA samples.

H. Rennert, J. Blumenfeld, Genyan Liu, 2014, Gene.

Novel method for genomic analysis of PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease

D. Leonard, H. Rennert, J. Blumenfeld, 2009, Human mutation.

Molecular diagnosis of autosomal dominant polycystic kidney disease using next-generation sequencing.

O. Elemento, H. Rennert, J. Blumenfeld, 2014, The Journal of molecular diagnostics : JMD.

A novel long-range PCR sequencing method for genetic analysis of the entire PKD1 gene.

H. Rennert, J. Blumenfeld, S. Donahue, 2012, The Journal of molecular diagnostics : JMD.

Aberrant PKD2 splicing due to a presumed novel missense mutation in autosomal‐dominant polycystic kidney disease

H. Rennert, J. Blumenfeld, S. Donahue, 2011, Clinical genetics.

Protocol for genetic testing in Huntington disease: three years of experience in Minnesota.

H. Orr, S. Rich, L. Heston, 1991, American journal of medical genetics.

Bmc Microbiology

B. Birren, W. Nierman, H. Kim, 2022 .