Retinitis pigmentosa, X-linked form: two kindreds

A multicenter, randomized phase 2 study to establish combinations of CBP501, cisplatin and nivolumab for ≥3rd-line treatment of patients with advanced pancreatic adenocarcinoma.

European journal of cancer (Oxford, England : 1990)·2024

Impact of baricitinib in combination with topical steroids on atopic dermatitis symptoms, quality of life and functioning in adult patients with moderate-to-severe atopic dermatitis from the BREEZE-AD7 Phase 3 randomized trial.

Journal of the European Academy of Dermatology and Venereology : JEADV·2021

Motion-induced interruptions and postural equilibrium in linear lateral accelerations.

Ergonomics·2014

The genetic code--more than just a table.

Cell biochemistry and biophysics·2009

General methodology for evaluating the adhesion force of drops and bubbles on solid surfaces.

Langmuir : the ACS journal of surfaces and colloids·2009

Managing faecal retention and incontinence in neurodisability.

British journal of nursing (Mark Allen Publishing)·2002

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Frontiers in genetics·2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

European journal of human genetics : EJHG·2026

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Nature communications·2026

A Case of Sotos Syndrome With Right Shoulder Disarticulation Due to a High-Grade Malignant Peripheral Nerve Sheath Tumor in the Right Arm and Shoulder.

Cureus·2026

The utilization of multiplex PCR with fragment analysis for carrier screening of spinal muscular atrophy.

Clinica chimica acta; international journal of clinical chemistry·2026

The Clinical Phenotype and Genetic Analysis of Monogenic Non Syndromic Obesity Caused by MC4R Gene Variation.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

Retinitis pigmentosa, X-linked form: two kindreds

Related Concept Videos

A multicenter, randomized phase 2 study to establish combinations of CBP501, cisplatin and nivolumab for ≥3rd-line treatment of patients with advanced pancreatic adenocarcinoma.

Impact of baricitinib in combination with topical steroids on atopic dermatitis symptoms, quality of life and functioning in adult patients with moderate-to-severe atopic dermatitis from the BREEZE-AD7 Phase 3 randomized trial.

Motion-induced interruptions and postural equilibrium in linear lateral accelerations.

The genetic code--more than just a table.

General methodology for evaluating the adhesion force of drops and bubbles on solid surfaces.

Managing faecal retention and incontinence in neurodisability.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

A Case of Sotos Syndrome With Right Shoulder Disarticulation Due to a High-Grade Malignant Peripheral Nerve Sheath Tumor in the Right Arm and Shoulder.

The utilization of multiplex PCR with fragment analysis for carrier screening of spinal muscular atrophy.

The Clinical Phenotype and Genetic Analysis of Monogenic Non Syndromic Obesity Caused by MC4R Gene Variation.

Related Experiment Videos

Retinitis pigmentosa, X-linked form: two kindreds

Related Concept Videos

Related Articles