Disease: Chromosome 9- partial monosomy 9p
- 12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?
- 9p partial monosomy and disorders of sex development: review and postulation of a pathogenetic mechanism
- A case of 9p partial monosomy syndrome
- A Meta-Analysis Evaluating Clinical Outcomes of Patients with Renal Cell Carcinoma Harboring Chromosome 9P Loss
- Chromosomal deletion of 9p21 is linked to poor patient prognosis in papillary and clear cell kidney cancer
- Entire FGF12 duplication by complex chromosomal rearrangements associated with West syndrome
- Genetic analysis of a case with a supernumerary marker derived from chromosome 9
- Genetic analysis of a family with 9q34.3 microdeletion and microduplication caused by abnormal chromosome balance structure
- Identification of a possible association of JAK2 in development of microphthalmia, anophthalmia, and coloboma (MAC) complex in a child with 9p deletion and duplication
- Inherited deletion of 9p22.3-p24.3 and duplication of 18p11.31-p11.32 associated with neurodevelopmental delay: Phenotypic matching of involved genes
- Loss of 9p21 Regulatory Hub Promotes Kidney Cancer Progression by Upregulating HOXB13
- Molecular cytogenetic characterization of a de novo derivative chromosome X with an unbalanced t(X;9) translocation in a fetus and literature review
- Partial deletion 9p syndrome in Malaysian children
- Partial trisomy 9p and partial monosomy 7p of an infant inherited from maternal balanced translocation: a case report
- Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions
- Precise breakpoint detection in a patient with 9p- syndrome
- Pure distal 9p deletion in a female infant with cerebral palsy
- Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome
- Ring chromosome formation by intra-strand repairing of subtelomeric double stand breaks and clinico-cytogenomic correlations for ring chromosome 9
- Risk prediction for metastasis of clear cell renal cell carcinoma using digital multiplex ligation-dependent probe amplification
- Sex discordance identification following non-invasive prenatal testing