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A new case of deletion 1q42 syndrome
E Tolkendorf1, G K Hinkel, A Gabriel
1Clinic of Gynecology and Obstetrics, Department of Clinical Genetics, Medical Academy Carl Gustav Carus, Dresden, German Democratic Republic.
Clinical Genetics
|April 1, 1989
Abstract:
We report a 1 8/12-year-old male with a de novo deletion of 1q42. The case is compared with 23 others from the literature. The clinical manifestations of our patient correspond with the phenotype of previous reports.