Chromosome 15q Deletion Latest Advances
Find the Latest Research About Chromosome 15q Deletion
Last Updated: 04/28/2026
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Found 14 publications
A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature.
Journal: BMC medical genomics
Published: December 06, 2019
Compulsions in Prader-Willi syndrome: occurrence and severity as a function of genetic subtype.
Journal: Actas espanolas de psiquiatria
Published: May 01, 2019
Apparent germline mosaicism for a 15q11-q13 deletion causing recurrent Angelman syndrome in a Chinese family.
Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: January 16, 2019
Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 24, 2016
A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS.
Journal: Genetic counseling (Geneva, Switzerland)
Published: May 20, 2016
15q13.3 duplication in two patients with childhood-onset schizophrenia.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: October 23, 2015
Decline of CSF orexin (hypocretin) levels in Prader-Willi syndrome.
Journal: American journal of medical genetics. Part A
Published: September 08, 2015
Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy: additional information.
Journal: American journal of medical genetics. Part A
Published: September 18, 2014
Chromosome microarray analysis: a case report of infertile brothers with CATSPER gene deletion.
Journal: Gene
Published: January 02, 2014
Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques.
Journal: BioMed research international
Published: October 26, 2012
Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci.
Journal: American journal of medical genetics. Part A
Published: June 06, 2012
An emerging phenotype of interstitial 15q25.2 microdeletions: clinical report and review.
Journal: American journal of medical genetics. Part A
Published: April 10, 2012
Last Updated: 04/28/2026