A mouse model for Fraser syndrome?

Same author

Mental health and wellbeing coordinators in primary schools to support student mental health: protocol for a quasi-experimental cluster study.

BMC public health·2021

Same author

Germ Line Deletion Reveals a Nonessential Role of Atypical Mitogen-Activated Protein Kinase 6/Extracellular Signal-Regulated Kinase 3.

Molecular and cellular biology·2019

Same author

The deubiquitylase Ataxin-3 restricts PTEN transcription in lung cancer cells.

Oncogene·2013

Same author

Optimum pH and temperature, and energy of activation of the transamination between glutamic acid and pyruvic acid.

Nature·2010

Same author

Aberrant regulation of imprinted gene expression in Gtl2lacZ mice.

Cytogenetic and genome research·2006

Same author

Neuropsychological evidence for separating components of visuo-spatial working memory.

Journal of neurology·2005

Same journal

A male infant with a novel heterogeneous nuclear ribonucleoprotein H1 variant, bilateral cataracts, dysplastic thumbs, and severe airway malacia.

Clinical dysmorphology·2026

Same journal

Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features.

Clinical dysmorphology·2026

Same journal

Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.

Clinical dysmorphology·2026

Same journal

A case of serpentine fibula-polycystic kidney syndrome presenting with foetal limb shortening: a disorder of foetal osteogenesis and part of the phenotypic spectrum of Hajdu-Cheney syndrome.

Clinical dysmorphology·2026

Same journal

Lateral nasal proboscis associated with nasal glioma: a complex unilateral craniofacial malformation.

Clinical dysmorphology·2026

Same journal

Primrose syndrome with a novel ZBTB20 variant with congenital glaucoma and hydrocephalus.

Clinical dysmorphology·2026

Related Experiment Videos

A mouse model for Fraser syndrome?

Related Concept Videos

Mental health and wellbeing coordinators in primary schools to support student mental health: protocol for a quasi-experimental cluster study.

Germ Line Deletion Reveals a Nonessential Role of Atypical Mitogen-Activated Protein Kinase 6/Extracellular Signal-Regulated Kinase 3.

The deubiquitylase Ataxin-3 restricts PTEN transcription in lung cancer cells.

Optimum pH and temperature, and energy of activation of the transamination between glutamic acid and pyruvic acid.

Aberrant regulation of imprinted gene expression in Gtl2lacZ mice.

Neuropsychological evidence for separating components of visuo-spatial working memory.

A male infant with a novel heterogeneous nuclear ribonucleoprotein H1 variant, bilateral cataracts, dysplastic thumbs, and severe airway malacia.

Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features.

Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.

A case of serpentine fibula-polycystic kidney syndrome presenting with foetal limb shortening: a disorder of foetal osteogenesis and part of the phenotypic spectrum of Hajdu-Cheney syndrome.

Lateral nasal proboscis associated with nasal glioma: a complex unilateral craniofacial malformation.

Primrose syndrome with a novel ZBTB20 variant with congenital glaucoma and hydrocephalus.

Related Experiment Videos

A mouse model for Fraser syndrome?

Related Concept Videos

Related Articles

Mental health and wellbeing coordinators in primary schools to support student mental health: protocol for a quasi-experimental cluster study.

Germ Line Deletion Reveals a Nonessential Role of Atypical Mitogen-Activated Protein Kinase 6/Extracellular Signal-Regulated Kinase 3.

The deubiquitylase Ataxin-3 restricts PTEN transcription in lung cancer cells.

Optimum pH and temperature, and energy of activation of the transamination between glutamic acid and pyruvic acid.

Aberrant regulation of imprinted gene expression in Gtl2lacZ mice.

Neuropsychological evidence for separating components of visuo-spatial working memory.

A male infant with a novel heterogeneous nuclear ribonucleoprotein H1 variant, bilateral cataracts, dysplastic thumbs, and severe airway malacia.

Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features.

Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.

A case of serpentine fibula-polycystic kidney syndrome presenting with foetal limb shortening: a disorder of foetal osteogenesis and part of the phenotypic spectrum of Hajdu-Cheney syndrome.

Lateral nasal proboscis associated with nasal glioma: a complex unilateral craniofacial malformation.

Primrose syndrome with a novel ZBTB20 variant with congenital glaucoma and hydrocephalus.