Cosegregation of T108A Elk-1 with mental retardation

Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes.

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[Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version].

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Recognizing the tenascin-X deficient type of Ehlers-Danlos syndrome: a cross-sectional study in 17 patients.

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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.

Molecular psychiatry·2016

Approaching theoretical strength in glassy carbon nanolattices.

Nature materials·2016

Novel insights into early embryonic demise via 3D surface rendered imaging in 107 cases.

Ultraschall in der Medizin (Stuttgart, Germany : 1980)·2014

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

Accuracy of Ultrasound-Estimated Epidural Depth in Transverse Median Versus Parasagittal Oblique Planes for Lower Thoracic Epidural Anesthesia: A Prospective Observational Comparative Study.

Cureus·2026

Under-Reporting of Drug Use in Douliu, Taiwan: Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) Screening Identifies Cases Beyond Education and Tattoo Markers in an Emergency Department Cohort.

Journal of acute medicine·2026

Genetically Proxied Leukocyte Telomere Length and Epigenetic Age Acceleration in Relation to Healthspan: A Mendelian Randomization Study.

Annals of human genetics·2026

Use of Whole Genome Sequencing to Investigate the Risk for Transmission of Clostridioides difficile From Prior Room Occupants: A Single-Center Study.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America·2026

Increasing Overall Rates of Prenatal Diagnosis Benefit Previously Disadvantaged Anatomic and Sociodemographic Subgroups.

Journal of the American Heart Association·2026

Emergency department referral and short-term death after outpatient hyperkalemia: a population-based study.

CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne·2026

Related Experiment Videos

Cosegregation of T108A Elk-1 with mental retardation

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Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes.

[Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version].

Recognizing the tenascin-X deficient type of Ehlers-Danlos syndrome: a cross-sectional study in 17 patients.

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.

Approaching theoretical strength in glassy carbon nanolattices.

Novel insights into early embryonic demise via 3D surface rendered imaging in 107 cases.

Defects of blastogenesis.

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

Limb anomalies: Developmental and evolutionary aspects.

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Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

Three cases of tetrasomy 9p.

Accuracy of Ultrasound-Estimated Epidural Depth in Transverse Median Versus Parasagittal Oblique Planes for Lower Thoracic Epidural Anesthesia: A Prospective Observational Comparative Study.

Under-Reporting of Drug Use in Douliu, Taiwan: Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) Screening Identifies Cases Beyond Education and Tattoo Markers in an Emergency Department Cohort.

Genetically Proxied Leukocyte Telomere Length and Epigenetic Age Acceleration in Relation to Healthspan: A Mendelian Randomization Study.

Use of Whole Genome Sequencing to Investigate the Risk for Transmission of Clostridioides difficile From Prior Room Occupants: A Single-Center Study.

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Cosegregation of T108A Elk-1 with mental retardation

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