Roosenboom J., Demaerel W., Breuls M., Appermont E., Claes P., Hammond P., Peeters H., Devriendt K., Hens G., ''Deletion of TBX1 is not responsible for facial dysmorphology in patients with 22q11.2 deletion syndrome'', Abstract book BeSHG & NVHG first joint meeting “Genetics & Society”, pp. 91, February 4-5, 2016, Leuven, Belgium.status: publishe
Abstract Background The heterozygous microdeletion of...
22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of th...
Structural variations in the chromosome 22q11.2 region medi-ated by nonallelic homologous recombinat...
Roosenboom J., Demaerel W., Breuls M., Appermont E., Claes P., Hammond P., Peeters H., Devriendt K.,...
Roosenboom J., Hens G., Lagae L., Claes P., Demaerel W., Swillen A., Vergaelen E., Breckpot J., Peet...
Background: Although TBX1 mutations have been identified in patients with 22q11.2 deletion syndrome ...
BACKGROUND: Although TBX1 mutations have been identified in patients with 22q11.2 deletion syndrome ...
<div><p>Background</p><p>Although <i>TBX1</i> mutations have been identified in patients with 22q11....
Bülent Hacihamdioğlu,1 Duygu Hacihamdioğlu,2 Kenan Delil3 1Department of Pediatric Endocrinolog...
Item does not contain fulltext22q11.2 deletion syndrome is one of the most common microdeletion synd...
22q11.2 deletion syndrome is one of the most common microdeletion syndromes. Most patients have a de...
Velo-cardio-facial syndrome/DiGeorge syndrome, also known as 22q11.2 deletion syndrome (22q11DS) is ...
The 22q11.2 chromosomal landscape predisposes to genomic rearrangements that are associated with a v...
Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a...
Haploinsufficiency of TBX1, encoding a T-box transcription factor, is largely responsible for the ph...
Abstract Background The heterozygous microdeletion of...
22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of th...
Structural variations in the chromosome 22q11.2 region medi-ated by nonallelic homologous recombinat...
Roosenboom J., Demaerel W., Breuls M., Appermont E., Claes P., Hammond P., Peeters H., Devriendt K.,...
Roosenboom J., Hens G., Lagae L., Claes P., Demaerel W., Swillen A., Vergaelen E., Breckpot J., Peet...
Background: Although TBX1 mutations have been identified in patients with 22q11.2 deletion syndrome ...
BACKGROUND: Although TBX1 mutations have been identified in patients with 22q11.2 deletion syndrome ...
<div><p>Background</p><p>Although <i>TBX1</i> mutations have been identified in patients with 22q11....
Bülent Hacihamdioğlu,1 Duygu Hacihamdioğlu,2 Kenan Delil3 1Department of Pediatric Endocrinolog...
Item does not contain fulltext22q11.2 deletion syndrome is one of the most common microdeletion synd...
22q11.2 deletion syndrome is one of the most common microdeletion syndromes. Most patients have a de...
Velo-cardio-facial syndrome/DiGeorge syndrome, also known as 22q11.2 deletion syndrome (22q11DS) is ...
The 22q11.2 chromosomal landscape predisposes to genomic rearrangements that are associated with a v...
Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a...
Haploinsufficiency of TBX1, encoding a T-box transcription factor, is largely responsible for the ph...
Abstract Background The heterozygous microdeletion of...
22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of th...
Structural variations in the chromosome 22q11.2 region medi-ated by nonallelic homologous recombinat...