Genetics casebook. X-linked dominant chrondrodyplasia punctata without stippled epiphyses

Absence of subcortical pathway optokinetic eye movements in an infant with cortical blindness.

Strabismus·2011

Comparison of latent nystagmus and nasotemporal asymmetries of optokinetic nystagmus in adult humans and macaque monkeys who have infantile strabismus.

Strabismus·2011

Weighted and unweighted comorbidity burden for predicting three-year neurodevelopment in extremely preterm infants: A nationwide cohort study.

Journal of perinatology : official journal of the California Perinatal Association·2026

Engaging families to improve high-risk infant follow-up participation: a mixed methods study.

Journal of perinatology : official journal of the California Perinatal Association·2026

Risk assessment of early-onset sepsis in extremely preterm infants: implications for antibiotic stewardship.

Journal of perinatology : official journal of the California Perinatal Association·2026

Exploring hope in parents of infants discharged from the neonatal intensive care unit: a cross-sectional study.

Journal of perinatology : official journal of the California Perinatal Association·2026

Diaphragm ultrasound and lung aeration in small-for-gestational-age versus appropriate-for-gestational-age newborns: a cross-sectional study.

Journal of perinatology : official journal of the California Perinatal Association·2026

Local anesthetic techniques for analgesia in neonatal circumcision: a network meta-analysis.

Journal of perinatology : official journal of the California Perinatal Association·2026

The Novel HLA-A*01:524 Allele With a Non-Synonymous Mutation in Exon 1 Identified in an Individual From North India.

HLA·2026

Triple carbapenemase-producing Klebsiella pneumoniae ST6668 resistant to novel β-lactam/β-lactamase inhibitor combinations and cefiderocol, Northern Italy, 2025.

International journal of antimicrobial agents·2026

Characterisation of the Novel HLA-DRB1*14:02:13 Allele by Sequencing-Based Typing.

HLA·2026

The Novel HLA-B*51:397 Allele, Identified by Sanger Dideoxy Nucleotide Sequencing in a Chinese Individual.

HLA·2026

Characterisation of the Novel HLA-C*08:334 Allele in a Brazilian Volunteer Donor.

HLA·2026

Identification of the Novel HLA-DQB1*05:385 Allele Through Next-Generation Sequencing.

HLA·2026

Related Experiment Videos

Genetics casebook. X-linked dominant chrondrodyplasia punctata without stippled epiphyses

Related Concept Videos

Absence of subcortical pathway optokinetic eye movements in an infant with cortical blindness.

Comparison of latent nystagmus and nasotemporal asymmetries of optokinetic nystagmus in adult humans and macaque monkeys who have infantile strabismus.

Weighted and unweighted comorbidity burden for predicting three-year neurodevelopment in extremely preterm infants: A nationwide cohort study.

Engaging families to improve high-risk infant follow-up participation: a mixed methods study.

Risk assessment of early-onset sepsis in extremely preterm infants: implications for antibiotic stewardship.

Exploring hope in parents of infants discharged from the neonatal intensive care unit: a cross-sectional study.

Diaphragm ultrasound and lung aeration in small-for-gestational-age versus appropriate-for-gestational-age newborns: a cross-sectional study.

Local anesthetic techniques for analgesia in neonatal circumcision: a network meta-analysis.

The Novel HLA-A*01:524 Allele With a Non-Synonymous Mutation in Exon 1 Identified in an Individual From North India.

Triple carbapenemase-producing Klebsiella pneumoniae ST6668 resistant to novel β-lactam/β-lactamase inhibitor combinations and cefiderocol, Northern Italy, 2025.

Characterisation of the Novel HLA-DRB1*14:02:13 Allele by Sequencing-Based Typing.

The Novel HLA-B*51:397 Allele, Identified by Sanger Dideoxy Nucleotide Sequencing in a Chinese Individual.

Characterisation of the Novel HLA-C*08:334 Allele in a Brazilian Volunteer Donor.

Identification of the Novel HLA-DQB1*05:385 Allele Through Next-Generation Sequencing.

Related Experiment Videos

Genetics casebook. X-linked dominant chrondrodyplasia punctata without stippled epiphyses

Related Concept Videos

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