Trisomy 5p in a prenatal case with ultrasound abnormalities

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Surgery, Octreotide, Temozolomide, Bevacizumab, Radiotherapy, and Pegvisomant Treatment of an AIP Mutation‒Positive Child.

The Journal of clinical endocrinology and metabolism·2019

The criminogenic and psychological effects of police stops on adolescent black and Latino boys.

Proceedings of the National Academy of Sciences of the United States of America·2019

Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia.

Indian journal of ophthalmology·2017

Deep Sequencing of Cell-Free Peripheral Blood DNA as a Reliable Method for Confirming the Diagnosis of Myelodysplastic Syndrome.

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After All I Have Done For You: Self-silencing Accommodations Fuel Women's Post-Rejection Hostility.

Journal of experimental social psychology·2013

Prenatal Genetic and Sonographic Features of KBG Syndrome: A Cohort Study of 19 Fetal Cases.

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Rare Autosomal Trisomies Detected by Noninvasive Prenatal Testing: Performance, Outcomes, and Exploratory Analysis of the Theoretical Mosaicism Ratio.

Prenatal diagnosis·2026

Multicentric Longitudinal Performance Monitoring of Different Prenatal Cell-Free DNA Screening Technologies in Belgium.

Prenatal diagnosis·2026

Maternal Sirolimus Therapy for Fetal Extensive Lymphatic Cystic Malformation: Selection Criteria, Management, and Outcomes in a Series of Six Cases.

Prenatal diagnosis·2026

When Fetal Anomalies Lead to Prognostic Clarification: An Underrecognized Application of Exome Sequencing.

Prenatal diagnosis·2026

Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

Prenatal diagnosis·2026

Expanding the diagnostic lens: Whole exome sequencing in a neonate with arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.

Journal of neonatal-perinatal medicine·2026

Severe Transfusion-Dependent Infantile Hemolytic Anemia Associated With a Novel Homozygous PKLR Variant of Uncertain Significance (c.1376C>G, p.Ala459Gly) and Coexisting G6PD Deficiency: A Case Report.

Cureus·2026

Stage-specific neutrophil states in neonatal injury: from antimicrobial deficiency to pro-resolution repair.

Frontiers in immunology·2026

Glycosylated Fibronectin in Fetal Growth Restriction: An Emerging Biomarker of Placental Dysfunction.

Cureus·2026

Palatoglossal Synechia in a Neonate Causing Severe Feeding Problems and Respiratory Distress: First Case Report from Somalia.

Pediatric health, medicine and therapeutics·2026

Idiopathic Epididymo-Orchitis and Pyocele in a Preterm Newborn: A Case Report.

Case reports in pediatrics·2026

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Trisomy 5p in a prenatal case with ultrasound abnormalities

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A Novel Splice Site Mutation in IFNGR2 in Patients With Primary Immunodeficiency Exhibiting Susceptibility to Mycobacterial Diseases.

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Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia.

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Prenatal Genetic and Sonographic Features of KBG Syndrome: A Cohort Study of 19 Fetal Cases.

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Trisomy 5p in a prenatal case with ultrasound abnormalities

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