Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference14 articles.
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2. Interstitial deletion del(17) (q21.3q23 or 24.2) syndrome
3. Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients
4. A Family with Hypogonadotropic Hypogonadism and Mutations in the Gonadotropin-Releasing Hormone Receptor
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2. Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder;Otology & Neurotology;2021-05-26
3. Multiple synostoses syndrome: Clinical report and retrospective analysis;American Journal of Medical Genetics Part A;2020-04-07
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5. Primary and Secondary Hypogonadism;Endocrinology;2017
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