Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH.

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22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro Fertilization.

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Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH.

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Unique Combination of 22q11 an ...... ing Oligonucleotide Array-CGH.

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Unique Combination of 22q11 an ...... ing Oligonucleotide Array-CGH.

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Unique Combination of 22q11 an ...... ing Oligonucleotide Array-CGH.

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Unique Combination of 22q11 an ...... sing Oligonucleotide Array-CGH

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I Slámová

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J Soukalová

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Siva-1 and an alternative splice form lacking the death domain, Siva-2, similarly induce apoptosis in T lymphocytes via a caspase-dependent mitochondrial pathway

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DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion

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TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

Bcl11b is required for differentiation and survival of alphabeta T lymphocytes

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

Delineation of 14q32.3 deletion syndrome.

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

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scholarly article

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10.1159/000335334

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Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH.

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P2860

P2860

Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH.

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