Prenatal diagnosis of a rare 1p36 heterochromatin variation with a ventricular septal defect in a twin pregnancy
Source: Egyptian Journal of Medical Human Genetics
Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion Syndrome
Source: Molecular Genetics and Genomic Medicine
Clinical Features of a Japanese Girl With Radio-Tartaglia Syndrome due to a SPEN Truncating Variant
Source: American Journal of Medical Genetics, Part A
Identification of De Novo Radio-Tartaglia Syndrome and Comparison of Clinical and Molecular Characteristics with Those of 1p36 Deletion Syndrome
Source: Annals of Child Neurology
Genetic Analysis of 1p36 Deletions for Six Aborted Fetuses
Source: Alternative Therapies in Health and Medicine
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