An Overview of Mongenic and Syndromic Obesities in Humans

Por Chung, Wendy K.
Publicado em 2011

The Process of Deciding About Prophylactic Surgery for Breast and Ovarian Cancer: Patient Questions, Uncertainties, and Communication

Por Klitzman, Robert, Chung, Wendy
Publicado em 2010

Quantitative Analysis of Copy Number Variants Based on Real-Time LightCycler PCR

Por Ma, Lijiang, Chung, Wendy K.
Publicado em 2014

The role of genetics in pulmonary arterial hypertension

Por Ma, Lijiang, Chung, Wendy K.
Publicado no J Pathol (2016)

Considerations Regarding the Genetics of Obesity

Por Chung, Wendy K., Leibel, Rudolph L.
Publicado em 2008

Incidental Findings in the Era of Whole Genome Sequencing?

Por PARENS, ERIK, APPELBAUM, PAUL, CHUNG, WENDY
Publicado em 2013

Return of Secondary Genomic Findings vs Patient Autonomy: Implications for Medical Care

Por Klitzman, Robert, Appelbaum, Paul S., Chung, Wendy
Publicado em 2013

Complex Genetics and the Etiology of Human Congenital Heart Disease

Por Gelb, Bruce D., Chung, Wendy K.
Publicado em 2014

Should Life Insurers Have Access to Genetic Test Results?

Por Klitzman, Robert, Appelbaum, Paul S., Chung, Wendy
Publicado no JAMA (2014)

Genetic Testing of Children for Diseases That Have Onset in Adulthood: The Limits of Family Interests

Por Hardart, George E., Chung, Wendy K.
Publicado no Pediatrics (2014)

Genetic causes of congenital diaphragmatic hernia

Por Wynn, Julia, Yu, Lan, Chung, Wendy K.
Publicado no Semin Fetal Neonatal Med (2014)

Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing

Por Coromilas, Alexandra, Wynn, Julia, Haverfield, Eden, Chung, Wendy K
Publicado no Clin Case Rep (2015)

Intragenic Deletion as a Novel Type of Mutation in Wolman Disease

Por Lee, Teresa M., Welsh, Mariko, Benhamed, Sonia, Chung, Wendy K.
Publicado em 2011

Cancer Genetic Counselor Information Needs for Risk Communication: A Qualitative Evaluation of Interview Transcripts

Por Overby, Casey Lynnette, Chung, Wendy K., Hripcsak, George, Kukafka, Rita
Publicado em 2013

Solid phase capturable dideoxynucleotides for multiplex genotyping using mass spectrometry

Por Kim, Sobin, Edwards, John R., Deng, Liyong, Chung, Wendy, Ju, Jingyue
Publicado em 2002

Similarity-based Disease Risk Assessment for Personal Genomes: Proof of Concept

Por Woo, Jung Hoon, Lai, Albert M., Chung, Wendy K., Weng, Chunhua
Publicado em 2011

Processes and factors involved in decisions regarding return of incidental genomic findings in research

Por Klitzman, Robert, Buquez, Brigitte, Appelbaum, Paul S., Fyer, Abby, Chung, Wendy K.
Publicado em 2013

The Expanding MEGDEL Phenotype: Optic Nerve Atrophy, Microcephaly, and Myoclonic Epilepsy in a Child with SERAC1 Mutations

Por Lumish, Heidi S., Yang, Yaping, Xia, Fan, Wilson, Ashley, Chung, Wendy K.
Publicado no JIMD Rep (2014)

Deep genetic connection between cancer and developmental disorders

Por Qi, Hongjian, Dong, Chengliang, Chung, Wendy K., Wang, Kai, Shen, Yufeng
Publicado no Hum Mutat (2016)

A unique case of der(11)t(11;22),−22 arising from 3 : 1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer

Por Jobanputra, Vaidehi, Chung, Wendy K., Hacker, April M., Emanuel, Beverly S., Warburton, Dorothy
Publicado em 2005