- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications ; day:24 ; month:7 ; year:2024 ; pages:1-9
Molecular psychiatry ; (24.7.2024), 1-9
- Urheber
-
Gur, Ruben C.
Bearden, Carrie E.
Jacquemont, Sebastien
Swillen, Ann
Amelsvoort, Therese van
Bree, Marianne van den
Vorstman, Jacob
Sebat, Jonathan
Ruparel, Kosha
Gallagher, Robert Sean
McClellan, Emily
White, Lauren
Crowley, Terrence Blaine
Giunta, Victoria
Kushan, Leila
O’Hora, Kathleen
Verbesselt, Jente
Vandensande, Ans
Vingerhoets, Claudia
Haelst, Mieke van
Hall, Jessica
Harwood, Janet
Chawner, Samuel J.R.A
Patel, Nishi
Palad, Katrina
Hong, Oanh
Guevara, James
Martin, Charles Olivier
Jizi, Khadije
Bélanger, Anne-Marie
Scherer, Stephen W.
Bassett, Anne S.
McDonald-McGinn, Donna M.
Gur, Raquel E.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41380-024-02661-y
- URN
-
urn:nbn:de:101:1-2410100731049.444542545208
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:38 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Gur, Ruben C.
- Bearden, Carrie E.
- Jacquemont, Sebastien
- Swillen, Ann
- Amelsvoort, Therese van
- Bree, Marianne van den
- Vorstman, Jacob
- Sebat, Jonathan
- Ruparel, Kosha
- Gallagher, Robert Sean
- McClellan, Emily
- White, Lauren
- Crowley, Terrence Blaine
- Giunta, Victoria
- Kushan, Leila
- O’Hora, Kathleen
- Verbesselt, Jente
- Vandensande, Ans
- Vingerhoets, Claudia
- Haelst, Mieke van
- Hall, Jessica
- Harwood, Janet
- Chawner, Samuel J.R.A
- Patel, Nishi
- Palad, Katrina
- Hong, Oanh
- Guevara, James
- Martin, Charles Olivier
- Jizi, Khadije
- Bélanger, Anne-Marie
- Scherer, Stephen W.
- Bassett, Anne S.
- McDonald-McGinn, Donna M.
- Gur, Raquel E.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
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
Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia
Generation of megabase-scale deletions, inversions and duplications involving the Contactin-6 gene in mice by CRISPR/Cas9 technology
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
Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
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
Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia
Generation of megabase-scale deletions, inversions and duplications involving the Contactin-6 gene in mice by CRISPR/Cas9 technology
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
Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
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
Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia
Generation of megabase-scale deletions, inversions and duplications involving the Contactin-6 gene in mice by CRISPR/Cas9 technology
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency