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American Journal of Medical Genetics. Part A|March 19, 2021
A case of Ververi-Brady syndrome due to QRICH1 loss of function and the literature reviewYoav Baruch, Shirley Horn-Saban, Yoram Plotsky, et al.
Frontiers in Endocrinology|July 19, 2019
Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to <i>POU1F1</i> MutationHussein Majdoub, Serge Amselem, Marie Legendre, et al.
Human Mutation|September 27, 2002
MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndromeYuval Yaron, Bruria Ben Zeev, Ruth Shomrat, et al.
The Prostate|April 7, 2006
Mutation screening and association study of the candidate prostate cancer susceptibility genes MSR1, PTEN, and KLF6Anat Bar-Shira, Noa Matarasso, Serena Rosner, et al.
Genetic Testing|July 30, 2003
Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi JewsOfer Lehavi, Orna Aizenstein, Dani Bercovich, et al.
The Israel Medical Association Journal : IMAJ|February 4, 2011
A protocol for genetic evaluation of patients with multiple colorectal adenomas and without evidence of APC gene mutationGuy Rosner, Paul Rozen, Dani Bercovich, et al.
Human Mutation|October 2, 2004
A paradigm for single nucleotide polymorphism analysis: the case of the acetylcholinesterase geneYehudit Hasin, Nili Avidan, Dani Bercovich, et al.
BMC Genomics|February 6, 2015
Dispersal of an ancient retroposon in the TP53 promoter of Bovidae: phylogeny, novel mechanisms, and potential implications for cow milk persistencyYaron Dekel, Yossy Machluf, Shifra Ben-Dor, et al.
Familial Cancer|November 11, 2010
Two BRCA1/2 founder mutations in Jews of Sephardic originMichal Sagi, Avital Eilat, Liat Ben Avi, et al.
Thyroid : Official Journal of the American Thyroid Association|June 17, 2016
Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene MutationYardena Tenenbaum-Rakover, Marc-Olivier Turgeon, Shira London, et al.
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