Pages that link to "Q43505829"
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The following pages link to Monozygotic twins with chromosome 22q11 deletion and discordant phenotype (Q43505829):
Displaying 14 items.
- 22q11 deletion syndrome: a genetic subtype of schizophrenia (Q33745688) (← links)
- Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome (Q33989539) (← links)
- Discovery of variants unmasked by hemizygous deletions (Q34132775) (← links)
- Genetic counselling for schizophrenia in the era of molecular genetics (Q34203058) (← links)
- Genetic insights into schizophrenia (Q34203064) (← links)
- Epigenetic contributors to the discordance of monozygotic twins (Q34830485) (← links)
- How many breaks do we need to CATCH on 22q11? (Q42587476) (← links)
- Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations (Q43075180) (← links)
- Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins (Q43147036) (← links)
- Course of psychopathology, cognition and neurobiological abnormality in schizophrenia: developmental origins and amelioration by antipsychotics? (Q48364671) (← links)
- Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndrome. (Q51901404) (← links)
- Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. (Q52118236) (← links)
- Tuberous sclerosis, polycystic kidney disease and mucolipidosis III gamma caused by a microdeletion unmasking a recessive mutation. (Q54982276) (← links)
- Molecular genetics of 22q11.2 deletion syndrome (Q58124159) (← links)