Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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2. Kallmann syndrome in a patient with Weiss–Kruszka syndrome and a de novo deletion in 9q31.2;European Journal of Endocrinology;2021-07-01
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4. Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions;American Journal of Medical Genetics Part A;2018-10-22
5. Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats;Journal of the Formosan Medical Association;2015-01
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