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Publications by W H Finley

Chromosome 1p Terminal Deletion: Report of New Findings and Confirmation of Two Characteristic Phenotypes.

Journal of Medical Genetics

English

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Deletion at Chromosome 10p11.23-P12.1 Defines Characteristic Phenotypes With Marked Midface Retrusion

Journal of Human Genetics

English

Terminal Deletion of the Chromosome 4q With Hemivertebra: Case Report

English

Deletion of the Short Arm of Chromosome 3: A Case Report With Necropsy Findings.

Journal of Medical Genetics

English

Chromosome 10q26 Deletion Syndrome: Two New Cases and a Review of the Literature

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

Deletion of Chromosome 2 (P11-P13): Case Report and Review.

Journal of Medical Genetics

English

Characteristic Findings of Alstrom Syndrome With a Case Report

Open Journal of Clinical Diagnostics

English

Terminal Deletion (14)(q32.3): A New Case.

Journal of Medical Genetics

English

Cryptic Terminal Deletion of Chromosome 9q34: A Novel Cause of Syndromic Obesity in Childhood?

Journal of Medical Genetics

English

Gonadal Mosaicism of Large Terminal De Novo Duplication and Deletion in Siblings With Variable Intellectual Disability Phenotypes

Molecular genetics & genomic medicine

Molecular Biology

English