Pages that link to "Q51909004"
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The following pages link to Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome "tiling path" BAC array in a girl with heart defect, cleft palate, and developmental delay (Q51909004):
Displaying 26 items.
- α-cardiac actin mutations produce atrial septal defects (Q24298075) (← links)
- Reduced ACTC1 Expression Might Play a Role in the Onset of Congenital Heart Disease by Inducing Cardiomyocyte Apoptosis (Q24304096) (← links)
- Large recurrent microdeletions associated with schizophrenia (Q24654741) (← links)
- Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts. (Q30394234) (← links)
- Meis2 is essential for cranial and cardiac neural crest development (Q30399251) (← links)
- Chromosomal aberrations as detected by array comparative genomic hybridization in early low-grade intraepithelial neoplasias of the breast (Q34015151) (← links)
- Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome. (Q34988773) (← links)
- Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome (Q36091184) (← links)
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures (Q36627230) (← links)
- Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs (Q36943622) (← links)
- Review and update of SPRED1 mutations causing Legius syndrome (Q38023296) (← links)
- Acute High-Dose X-Radiation-Induced Genomic Changes in A549 Cells (Q38440129) (← links)
- De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux (Q38844455) (← links)
- Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway (Q39214917) (← links)
- Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population (Q41693961) (← links)
- Changes of gene expression profiles in the cervical spinal cord by acupuncture in an MPTP-intoxicated mouse model: Microarray analysis (Q43463927) (← links)
- Association between a single-nucleotide polymorphism in the GREM1 gene and non-syndromic orofacial cleft in the Chinese population (Q48281020) (← links)
- Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature (Q49779883) (← links)
- Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes. (Q51902875) (← links)
- Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability. (Q52648916) (← links)
- Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate. (Q52681596) (← links)
- Identification of SPRED1 deletions using RT-PCR, multiplex ligation-dependent probe amplification and quantitative PCR. (Q54374377) (← links)
- Is Chromosome 15q13.3 Duplication Involving CHRNA7 Associated With Oral Clefts? (Q55081756) (← links)
- An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype. (Q55507993) (← links)
- Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability (Q57021667) (← links)
- Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects (Q58749774) (← links)