Pages that link to "Q57813361"
Jump to navigation
Jump to search
The following pages link to Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region (Q57813361):
Displaying 50 items.
- Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome (Q24311578) (← links)
- Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans (Q24312613) (← links)
- Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome (Q24317602) (← links)
- Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11 (Q24322620) (← links)
- Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene (Q24324759) (← links)
- Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene (Q24626754) (← links)
- Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome (Q28209453) (← links)
- Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements (Q33608641) (← links)
- Chromosome 22q11 deletion presenting as the Potter sequence (Q33678881) (← links)
- Prenatal diagnosis by FISH of a 22q11 deletion in two families (Q33680264) (← links)
- A mother with VCFS and unilateral dysplastic kidney and her fetus with multicystic dysplastic kidneys: additional evidence to support the association of renal malformations and VCFS. (Q33680641) (← links)
- Phenotype of adults with the 22q11 deletion syndrome: A review (Q33736688) (← links)
- 22q11 deletion syndrome: a genetic subtype of schizophrenia (Q33745688) (← links)
- Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes (Q33944592) (← links)
- Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study (Q34063057) (← links)
- Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome (Q34145963) (← links)
- Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review (Q34242739) (← links)
- Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions (Q34305522) (← links)
- Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders. (Q35238706) (← links)
- Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients (Q35249478) (← links)
- Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. (Q35809309) (← links)
- Deletion mapping of 22q11 in CATCH22 syndrome: identification of a second critical region. (Q35882793) (← links)
- New findings from genetic association studies of schizophrenia (Q37374232) (← links)
- Otitis Media in Children with Congenital Immunodeficiencies (Q37782573) (← links)
- MicroRNAs in Schizophrenia: Implications for Synaptic Plasticity and Dopamine-Glutamate Interaction at the Postsynaptic Density. New Avenues for Antipsychotic Treatment Under a Theranostic Perspective. (Q38267957) (← links)
- Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcome. (Q38977130) (← links)
- Associations of common copy number variants in glutathione S-transferase mu 1 and D-dopachrome tautomerase-like protein genes with risk of schizophrenia in a Japanese population (Q40736341) (← links)
- Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot. (Q40986085) (← links)
- Deletion of 22q11 in two brothers with different phenotype (Q41063814) (← links)
- A Patient with 22q11.2 Deletion Syndrome: case report (Q41288717) (← links)
- Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician (Q41471214) (← links)
- Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH. (Q41934041) (← links)
- Simultaneous, Multilocus FISH Analysis for Detection of Microdeletions in the Diagnostic Evaluation of Developmental Delay and Mental Retardation (Q42284864) (← links)
- How many breaks do we need to CATCH on 22q11? (Q42587476) (← links)
- Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. (Q42678770) (← links)
- Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia (Q50542429) (← links)
- Clinical features of 78 adults with 22q11 Deletion Syndrome (Q51925287) (← links)
- Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk (Q51957860) (← links)
- Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method. (Q52120688) (← links)
- Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian children. (Q52142489) (← links)
- Another critical region for deletion of 22q11: A study of 100 patients (Q52192462) (← links)
- Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects (Q56977908) (← links)
- A common region of 10p deleted in DiGeorge and velocardiofacial syndromes (Q57251931) (← links)
- Schizophrenia and Hypocalcaemia: Variable Phenotype of Deletion at Chromosome 22q11 (Q58492826) (← links)
- Tricuspid atresia and 22q11 deletion (Q58924000) (← links)
- Transient congenital hypoparathyroidism: resolution and recurrence in chromosome 22q11 deletion (Q71050039) (← links)
- What's in a name? Chromosome 22q abnormalities and the DiGeorge, velocardiofacial, and conotruncal anomalies face syndromes (Q71788840) (← links)
- Conotruncal heart defects and chromosome 22q11 microdeletion (Q73236494) (← links)
- Unbalanced 15;22 translocation in a patient with manifestations of DiGeorge and velocardiofacial syndrome (Q73294029) (← links)
- Identification of Y chromatin directly in gonadal tissue by fluorescence in situ hybridization (FISH): significance for Ullrich-Turner syndrome screening in the cytogenetics laboratory (Q73680977) (← links)