Index of suspicion. Case 1. Diagnosis: Klinefelter syndrome

Respiratory epithelial cell invasion by group B streptococci.

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Psychiatrists and their patients--confidential information in the wake of spycatcher.

The Australian and New Zealand journal of psychiatry·1992

Immunotherapy with a tumor-infiltrating lymphocyte clone, soluble antigen, and cyclophosphamide.

Archives of surgery (Chicago, Ill. : 1960)·1992

Incidental finding of endolymphatic stromal myosis during luteinizing hormone releasing hormone agonist therapy for suspected benign uterine myomata. A case report.

The Journal of reproductive medicine·1992

Submicrometer intracellular chemical optical fiber sensors.

Science (New York, N.Y.)·1992

The esterification of fatty acids by Staphylococcus aureus fatty acid modifying enzyme (FAME) and its inhibition by glycerides.

Journal of medical microbiology·1992

Peptic Ulcer Disease in Pediatrics: A Comprehensive Review.

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Beyond Survival: Outpatient Treatment for Functional Recovery After Brain Injury.

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Something Doesn't Look Right: Recognizing and Managing Limb-Length Discrepancy.

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Hantavirus Infections in Children.

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Childhood Attachment Patterns and Disorders.

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Hemangiomas: Beyond the Skin.

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Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

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Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

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First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Mitochondrial DNA. Part B, Resources·2026

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

International journal of legal medicine·2026

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

Phlebology·2026

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

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Index of suspicion. Case 1. Diagnosis: Klinefelter syndrome

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Respiratory epithelial cell invasion by group B streptococci.

Psychiatrists and their patients--confidential information in the wake of spycatcher.

Immunotherapy with a tumor-infiltrating lymphocyte clone, soluble antigen, and cyclophosphamide.

Incidental finding of endolymphatic stromal myosis during luteinizing hormone releasing hormone agonist therapy for suspected benign uterine myomata. A case report.

Submicrometer intracellular chemical optical fiber sensors.

The esterification of fatty acids by Staphylococcus aureus fatty acid modifying enzyme (FAME) and its inhibition by glycerides.

Peptic Ulcer Disease in Pediatrics: A Comprehensive Review.

Beyond Survival: Outpatient Treatment for Functional Recovery After Brain Injury.

Something Doesn't Look Right: Recognizing and Managing Limb-Length Discrepancy.

Hantavirus Infections in Children.

Childhood Attachment Patterns and Disorders.

Hemangiomas: Beyond the Skin.

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

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Index of suspicion. Case 1. Diagnosis: Klinefelter syndrome

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