Can we rely on the family history?

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The Effect of Genetic Counseling on Knowledge and Perceptions Regarding Risks for Breast Cancer.

Journal of genetic counseling·2015

Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans.

Journal of medical genetics·2010

A mutation analysis of the phenylalanine hydroxylase (PAH) gene in the Israeli population.

Annals of human genetics·2008

The fate of 12 recessive mutations in a single village.

Annals of human genetics·2007

Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.

Hearing research·2003

Defects of blastogenesis.

American journal of medical genetics·2002

Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.

American journal of medical genetics·2002

Limb anomalies: Developmental and evolutionary aspects.

American journal of medical genetics·2002

Molecular etiology of gut malformations and diseases.

American journal of medical genetics·2002

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

American journal of medical genetics·2002

Three cases of tetrasomy 9p.

American journal of medical genetics·2002

What Survivors Remembered: Cognitive and Experiential Themes in Trauma Narratives From the Deadliest Mass Shooting in Modern American History.

Psychological science·2026

Lost in transmission? Comparing emotional profiles in transmitted vs. remembered family memories.

Memory (Hove, England)·2026

Joint changes in subjective memory and objective cognition and risk of incident functional dependence: A harmonized analysis of four aging cohorts.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

Beyond the arcsine law: Aging statistics of the occupation time in jump processes.

Physical review. E·2026

Hair cortisol and other analytes continue to decline and show reduced stability after two years of storage: Follow-up data from a systematic within-subject investigation.

Comprehensive psychoneuroendocrinology·2026

Assessment of variation in symphyseal morphology among Middle Stone Age hominin mandibles from Klasies River Main Site, South Africa, by diffeomorphic surface mapping.

Anatomical record (Hoboken, N.J. : 2007)·2026

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Monitoring public interest toward pertussis outbreaks: an extensive Google Trends-based analysis.

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Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans.

A mutation analysis of the phenylalanine hydroxylase (PAH) gene in the Israeli population.

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