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Diagnostic testing for rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene : Identification of several novel mutations and polymorphismsBUYSE, Inge M; PING FANG; HOON, Katherine T et al.American journal of human genetics. 2000, Vol 67, Num 6, pp 1428-1436, issn 0002-9297Article

Comprehensive Sequencing of PALB2 in Patients With Breast Cancer Suggests PALB2 Mutations Explain a Subset of Hereditary Breast CancerFERNANDES, Priscilla H; SAAM, Jennifer; PETERSON, Jenny et al.Cancer. 2014, Vol 120, Num 7, pp 963-967, issn 0008-543X, 5 p.Article

DNA sequence analysis of GJB2, encoding connexin 26: Observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controlsTANG, Hsiao-Yuan; PING FANG; WARD, Patricia A et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 22, pp 2401-2415, issn 1552-4825, 15 p.Article

Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assayBISWAS, Kajal; DAS, Ranabir; PRUSS, Dmitry et al.Human molecular genetics (Print). 2012, Vol 21, Num 18, pp 3993-4006, issn 0964-6906, 14 p.Article

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10MATSUURA, Tohru; PING FANG; ZOGHBI, Huda Y et al.American journal of human genetics. 2004, Vol 74, Num 6, pp 1216-1224, issn 0002-9297, 9 p.Article

Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15ABRAMS, Debra J; ARONOFF, Amy R; BEREND, Sue Ann et al.Prenatal diagnosis. 2001, Vol 21, Num 8, pp 676-679, issn 0197-3851Article

Angiotensinogen and endothelial nitric oxide synthase gene polymorphisms among Hispanic patients with preeclampsia. DiscussionBASHFORD, Michael T; HEFLER, Lukas A; VERTREES, Thomas W et al.American journal of obstetrics and gynecology. 2001, Vol 184, Num 7, pp 1345-1351, issn 0002-9378Conference Paper

Clinical Significance of Large Rearrangements in BRCA1 and BRCA2JUDKINS, Thaddeus; ROSENTHAL, Eric; ARNELL, Christopher et al.Cancer. 2012, Vol 118, Num 21, pp 5210-5216, issn 0008-543X, 7 p.Article

Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10 : Repeat purity as a disease modifier?MATSUURA, Tohru; PING FANG; PEARSON, Christopher E et al.American journal of human genetics. 2006, Vol 78, Num 1, pp 125-129, issn 0002-9297, 5 p.Article

Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption : CDAGSMENDOZA-LONDONO, Roberto; LAMMER, Edward; HEDGE, Madhuri R et al.American journal of human genetics. 2005, Vol 77, Num 1, pp 161-168, issn 0002-9297, 8 p.Article

Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathyTAKASHIMA, Hiroshi; BOERKOEL, Cornelius F; STOCKTON, David W et al.Nature genetics. 2002, Vol 32, Num 2, pp 267-272, issn 1061-4036, 6 p.Article

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