Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications ; volume:8 ; number:1 ; day:02 ; month:4 ; year:2007 ; pages:1-16 ; date:12.2007
BMC medical genetics ; 8, Heft 1 (02.4.2007), 1-16, 12.2007
- Creator
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Torres-Juan, Laura
- Contributor
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Rosell, Jordi
Sánchez-de-la-Torre, Manuel
Fibla, Joan
Heine-Suñer, Damià
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-8-14
- URN
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urn:nbn:de:1111-2016021833674
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:21 AM CEST
Data provider
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Associated
- Torres-Juan, Laura
- Rosell, Jordi
- Sánchez-de-la-Torre, Manuel
- Fibla, Joan
- Heine-Suñer, Damià
- SpringerLink (Online service)
Other Objects (12)
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications
Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
Sorting by reversals, block interchanges, tandem duplications, and deletions
An effect of large-scale deletions and duplications on transcript expression
DNA sequence features underlying large-scale duplications and deletions in human
Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
Very Low Rates of Spontaneous Gene Deletions and Gene Duplications in Dictyostelium discoideum
Parental origin of deletions and duplications – about the necessity to check for cryptic inversions
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency
Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia
Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia
Angstgeneralisierung bei Deletionssyndrom 22q11.2
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications
Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
Sorting by reversals, block interchanges, tandem duplications, and deletions
An effect of large-scale deletions and duplications on transcript expression
DNA sequence features underlying large-scale duplications and deletions in human
Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
Very Low Rates of Spontaneous Gene Deletions and Gene Duplications in Dictyostelium discoideum
Parental origin of deletions and duplications – about the necessity to check for cryptic inversions
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency
Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia
Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia
Angstgeneralisierung bei Deletionssyndrom 22q11.2
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications
Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
Sorting by reversals, block interchanges, tandem duplications, and deletions
An effect of large-scale deletions and duplications on transcript expression
DNA sequence features underlying large-scale duplications and deletions in human
Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
Very Low Rates of Spontaneous Gene Deletions and Gene Duplications in Dictyostelium discoideum
Parental origin of deletions and duplications – about the necessity to check for cryptic inversions
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency
Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia
Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia