A genetic study of syndactyly in Utah

Unsatisfactory results in augmentation mammoplasty: Chest and breast asymmetry.

Aesthetic plastic surgery·2013

Does the genotype for schizophrenia often remain unexpressed because of canalization and stochastic events during development?

Psychological medicine·1997

Directional and anteroposterior asymmetry of common white markings in the legs of the Arabian horse: response to selection.

Genetica·1997

Influence of stochastic events on the phenotypic variation of common white leg markings in the Arabian horse: implications for various genetic disorders in humans.

The Journal of heredity·1995

Developing a district diabetic register.

BMJ (Clinical research ed.)·1992

Common white facial markings in bay and chestnut Arabian horses and their hybrids.

The Journal of heredity·1991

Disparities in Disability Life Expectancy in US Birth Cohorts: The Influence of Sex and Race.

Social biology·2015

Are men really that bad as fathers? The role of men's investments.

Social biology·2011

Hunting, social status and biological fitness.

Social biology·2011

Historical and life course timing of the male mortality disadvantage in Europe: epidemiologic transitions, evolution, and behavior.

Social biology·2011

Men with subnormal sperm counts live shorter lives.

Social biology·2011

Age-related patterns of urinary gonadotropins (FSH and LH) and E-3-G as measures of reproductive function among Turkana males of northern Kenya.

Social biology·2011

Neuropathologic Features of Adult-Onset Progressive Leukodystrophy Due to KARS Pathogenic Variants: A Case Report.

Neurology. Genetics·2026

Unmasked Behavioral Disturbance Following Traumatic Brain Injury in an Adult With Previously Undiagnosed Sotos Syndrome.

Cureus·2026

Genetic profile of motor neuron disease in a multiregional Brazilian cohort: an 18-year real-world experience in 1,911 patients.

Frontiers in neurology·2026

Distinct neurogenic progenitor cell populations balance cell type production in the embryonic mouse retina.

bioRxiv : the preprint server for biology·2026

Biallelic protein truncating EXOSC6 variants cause a neurodevelopmental disorder with cerebellar atrophy, ataxia, and global developmental delay.

medRxiv : the preprint server for health sciences·2026

Germline NF2 variant position constrains somatic second hits and determines clinical severity in Neurofibromatosis Type 2-related schwannomatosis.

medRxiv : the preprint server for health sciences·2026

Related Experiment Videos

A genetic study of syndactyly in Utah

Related Concept Videos

Unsatisfactory results in augmentation mammoplasty: Chest and breast asymmetry.

Does the genotype for schizophrenia often remain unexpressed because of canalization and stochastic events during development?

Directional and anteroposterior asymmetry of common white markings in the legs of the Arabian horse: response to selection.

Influence of stochastic events on the phenotypic variation of common white leg markings in the Arabian horse: implications for various genetic disorders in humans.

Developing a district diabetic register.

Common white facial markings in bay and chestnut Arabian horses and their hybrids.

Disparities in Disability Life Expectancy in US Birth Cohorts: The Influence of Sex and Race.

Are men really that bad as fathers? The role of men's investments.

Hunting, social status and biological fitness.

Historical and life course timing of the male mortality disadvantage in Europe: epidemiologic transitions, evolution, and behavior.

Men with subnormal sperm counts live shorter lives.

Age-related patterns of urinary gonadotropins (FSH and LH) and E-3-G as measures of reproductive function among Turkana males of northern Kenya.

Neuropathologic Features of Adult-Onset Progressive Leukodystrophy Due to KARS Pathogenic Variants: A Case Report.

Unmasked Behavioral Disturbance Following Traumatic Brain Injury in an Adult With Previously Undiagnosed Sotos Syndrome.

Genetic profile of motor neuron disease in a multiregional Brazilian cohort: an 18-year real-world experience in 1,911 patients.

Distinct neurogenic progenitor cell populations balance cell type production in the embryonic mouse retina.

Biallelic protein truncating EXOSC6 variants cause a neurodevelopmental disorder with cerebellar atrophy, ataxia, and global developmental delay.

Germline NF2 variant position constrains somatic second hits and determines clinical severity in Neurofibromatosis Type 2-related schwannomatosis.

Related Experiment Videos

A genetic study of syndactyly in Utah

Related Concept Videos

Related Articles