Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis

Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.

Human genetics·1986

The fragile X in cattle.

American journal of medical genetics·1986

Detection and interpretation of two different cell lines in triploid abortions.

Clinical genetics·1985

Trisomy 21 Down syndrome. Parental mosaicism.

Human genetics·1985

Triploidy and chromosomes.

American journal of obstetrics and gynecology·1985

Twinning rate in spontaneous abortions.

American journal of human genetics·1983

School-Based Health and Healthcare Utilization Among Rural Youth: Evidence from a School-Based Health Center Opening.

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Outpatient Respiratory Outcomes in Infants Who Survive Hospitalization for Extreme Prematurity.

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Magnetic Resonance Imaging During Therapeutic Hypothermia Accurately Reflects the Degree of Brain Injury in Neonates with Hypoxic-Ischemic Encephalopathy.

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Acute Emotional Symptoms Predict Emotional Functioning Up to 6 Months After Pediatric Concussion: An A-CAP Study.

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Analytical Life Cycle Assessment as a 10-Stage Framework for Evaluating and Improving the Sustainability of Analytical Workflows.

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Validation of a standardized quantitative RT-qPCR workflow for detection and quantification of airborne respiratory viruses using gelatin membranes as sampling matrix.

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The College of American Pathologists (CAP) Laboratory Accreditation Program (LAP): Accreditation Process and its Impact on Laboratory Practice and Patient Safety.

EJIFCC·2026

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Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by

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Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.

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Detection and interpretation of two different cell lines in triploid abortions.

Trisomy 21 Down syndrome. Parental mosaicism.

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Twinning rate in spontaneous abortions.

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Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by