Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)

The Amish: Perceptions of genetic disorders and services.

Journal of genetic counseling·2013

Transform method of processing for speckle strain-rate measurements.

Applied optics·2010

Performance of a gradient-based shift estimator in a spatially sparse data environment: tracking the sub-pixel motion of fluorescent particles.

Journal of microscopy·2008

Acoustically modulated speckle imaging of biological tissues.

Optics letters·2007

Mechanical properties of coagulated albumin and failure mechanisms of liver repaired with the use of an argon-beam coagulator with albumin.

Journal of biomedical materials research·2002

Processing algorithms for tracking speckle shifts in optical elastography of biological tissues.

Journal of biomedical optics·2001

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

Mixed Presentation of Hyperglycemic Hyperosmolar State and Diabetic Ketoacidosis in a Pediatric Patient: a Case Report and Literature Review.

Journal of clinical research in pediatric endocrinology·2026

Renin-Aldosterone Activation and Enhanced Urinary Potassium Excretion in Asphyxiated Newborns Treated with Therapeutic Hypothermia: A Prospective Study.

Therapeutic hypothermia and temperature management·2026

Population pharmacokinetics of levetiracetam in term neonates with hypoxic-ischemic encephalopathy and therapeutic hypothermia: The LEVNEONAT-1 study.

British journal of clinical pharmacology·2026

Intubation videoendoscopy in a preterm infant with congenital tracheal stenosis and laryngotracheoesophageal cleft: a case report.

BMC pediatrics·2026

Incidence and predictors of early neonatal mortality among neonates admitted to neonatal intensive care units in public general hospitals in Northwest Ethiopia: a multicenter prospective cohort study.

BMC pediatrics·2026

Loss of protein function resulting in severe phenotypes of X-linked myotubular myopathy caused by novel synonymous and splice-site variants in the MTM1 gene.

Pediatrics and neonatology·2026

Related Experiment Videos

Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)

Related Concept Videos

The Amish: Perceptions of genetic disorders and services.

Transform method of processing for speckle strain-rate measurements.

Performance of a gradient-based shift estimator in a spatially sparse data environment: tracking the sub-pixel motion of fluorescent particles.

Acoustically modulated speckle imaging of biological tissues.

Mechanical properties of coagulated albumin and failure mechanisms of liver repaired with the use of an argon-beam coagulator with albumin.

Processing algorithms for tracking speckle shifts in optical elastography of biological tissues.

Defects of blastogenesis.

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

Limb anomalies: Developmental and evolutionary aspects.

Molecular etiology of gut malformations and diseases.

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

Three cases of tetrasomy 9p.

Mixed Presentation of Hyperglycemic Hyperosmolar State and Diabetic Ketoacidosis in a Pediatric Patient: a Case Report and Literature Review.

Renin-Aldosterone Activation and Enhanced Urinary Potassium Excretion in Asphyxiated Newborns Treated with Therapeutic Hypothermia: A Prospective Study.

Population pharmacokinetics of levetiracetam in term neonates with hypoxic-ischemic encephalopathy and therapeutic hypothermia: The LEVNEONAT-1 study.

Intubation videoendoscopy in a preterm infant with congenital tracheal stenosis and laryngotracheoesophageal cleft: a case report.

Incidence and predictors of early neonatal mortality among neonates admitted to neonatal intensive care units in public general hospitals in Northwest Ethiopia: a multicenter prospective cohort study.

Loss of protein function resulting in severe phenotypes of X-linked myotubular myopathy caused by novel synonymous and splice-site variants in the MTM1 gene.

Related Experiment Videos

Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)

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