我想悬赏1000积分找如下文献： 1、SETD5Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome
2、16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the Literature
3、Dual genetic diagnoses: neurofibromatosis type 1 and KBG syndrome
4、Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape