![Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series - ScienceDirect Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1028455921000012-gr1.jpg)
Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series - ScienceDirect
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Westerlay Orchids to host fundraiser to help support individuals suffering from rare genetic disorder | Home & Garden | lompocrecord.com
![PDF) Hypertriglyceridemia as a main feature associated with 17q12 deletion syndrome-related hepatocyte nuclear factor 1β-maturity-onset diabetes of the young PDF) Hypertriglyceridemia as a main feature associated with 17q12 deletion syndrome-related hepatocyte nuclear factor 1β-maturity-onset diabetes of the young](https://i1.rgstatic.net/publication/363582550_Hypertriglyceridemia_as_a_main_feature_associated_with_17q12_deletion_syndrome-related_hepatocyte_nuclear_factor_1b-maturity-onset_diabetes_of_the_young/links/6323a475071ea12e36370984/largepreview.png)
PDF) Hypertriglyceridemia as a main feature associated with 17q12 deletion syndrome-related hepatocyte nuclear factor 1β-maturity-onset diabetes of the young
![Cureus | 17q12 Microdeletion Syndrome as a Rare Cause of Elevated Liver Enzymes: Case Report and Literature Review | Article Cureus | 17q12 Microdeletion Syndrome as a Rare Cause of Elevated Liver Enzymes: Case Report and Literature Review | Article](https://assets.cureus.com/uploads/figure/file/496089/lightbox_c97785f0614311edb83cdd6762044329-IMG_3405-1-.png)
Cureus | 17q12 Microdeletion Syndrome as a Rare Cause of Elevated Liver Enzymes: Case Report and Literature Review | Article
![PDF) Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia PDF) Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia](https://www.researchgate.net/profile/Shuwen-Huang/publication/47699667/figure/fig4/AS:669652904579093@1536669102715/Facial-Phenotype-of-Patients-with-17q12-Deletions-Macrocephaly-epicanthal-folds_Q320.jpg)
PDF) Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
![Cureus | 17q12 Microdeletion Syndrome as a Rare Cause of Elevated Liver Enzymes: Case Report and Literature Review | Article Cureus | 17q12 Microdeletion Syndrome as a Rare Cause of Elevated Liver Enzymes: Case Report and Literature Review | Article](https://assets.cureus.com/uploads/figure/file/484687/lightbox_8e541af0530211ed93e24fbe019f63a3-us.png)
Cureus | 17q12 Microdeletion Syndrome as a Rare Cause of Elevated Liver Enzymes: Case Report and Literature Review | Article
![Recurrent 17q12 microduplications contribute to renal disease but not diabetes | Journal of Medical Genetics Recurrent 17q12 microduplications contribute to renal disease but not diabetes | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/early/2022/09/15/jmg-2022-108615/F3.large.jpg)
Recurrent 17q12 microduplications contribute to renal disease but not diabetes | Journal of Medical Genetics
![Expression quantitative trait locus fine mapping of the 17q12–21 asthma locus in African American children: a genetic association and gene expression study - The Lancet Respiratory Medicine Expression quantitative trait locus fine mapping of the 17q12–21 asthma locus in African American children: a genetic association and gene expression study - The Lancet Respiratory Medicine](https://www.thelancet.com/cms/attachment/b9d68d35-8b1c-4de1-b462-2c46dd6c9b94/gr1_lrg.jpg)
Expression quantitative trait locus fine mapping of the 17q12–21 asthma locus in African American children: a genetic association and gene expression study - The Lancet Respiratory Medicine
![Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 | European Journal of Human Genetics Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 | European Journal of Human Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fejhg.2009.174/MediaObjects/41431_2010_Article_BFejhg2009174_Fig1_HTML.jpg)
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 | European Journal of Human Genetics
17q12 Foundation - 17q12 Foundation represents two separate syndromes; 17q12 deletion syndrome and 17q12 duplication syndrome. Both syndromes involve the same 15 genes located on chromosome 17q12, but they are different syndromes
![Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion | Clinical Epigenetics | Full Text Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion | Clinical Epigenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13148-018-0530-z/MediaObjects/13148_2018_530_Fig2_HTML.png)