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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...American journal of human genetics, 2017-10, Vol.101 (4), p.616-622
2017
Volltextzugriff (PDF)
American journal of human genetics, 2018-09, Vol.103 (3), p.457-457
- Demaerel, Wolfram
- Hestand, Matthew S.
- Vergaelen, Elfi
- Swillen, Ann
- López-Sánchez, Marcos
- Pérez-Jurado, Luis A.
- McDonald-McGinn, Donna M.
- Zackai, Elaine
- Emanuel, Beverly S.
- Morrow, Bernice E.
- Breckpot, Jeroen
- Devriendt, Koenraad
- Vermeesch, Joris R.
- Antshel, Kevin
- Arango, Celso
- Armando, Marco
- Bassett, Anne
- Bearden, Carrie
- Boot, Erik
- Bravo-Sanchez, Marta
- Breetvelt, Elemi
- Busa, Tiffany
- Butcher, Nancy
- Campbell, Linda
- Carmel, Miri
- Chow, Eva
- Crowley, T. Blaine
- Cubells, Joseph
- Cutler, David
- Digilio, Maria Cristina
- Duijff, Sasja
- Eliez, Stephan
- Emanuel, Beverly
- Epstein, Michael
- Evers, Rens
- Fernandez Garcia-Moya, Luis
- Fiksinski, Ania
- Fraguas, David
- Fremont, Wanda
- Fritsch, Rosemarie
- Garcia-Minaur, Sixto
- Golden, Aaron
- Gothelf, Doron
- Guo, Tingwei
- Gur, Ruben
- Gur, Raquel
- Heine-Suner, Damian
- Hestand, Matthew
- Hooper, Stephen
- Kates, Wendy
- Kushan, Leila
- Laorden-Nieto, Alejandra
- Maeder, Johanna
- Marino, Bruno
- Marshall, Christian
- McCabe, Kathryn
- McDonald-McGinn, Donna
- Michaelovosky, Elena
- Morrow, Bernice
- Moss, Edward
- Mulle, Jennifer
- Murphy, Declan
- Murphy, Kieran
- Murphy, Clodagh
- Niarchou, Maria
- Ornstein, Claudia
- Owen, Michael
- Philip, Nicole
- Repetto, Gabriela
- Schneider, Maude
- Shashi, Vandana
- Simon, Tony
- Tassone, Flora
- Unolt, Marta
- van Amelsvoort, Therese
- van den Bree, Marianne
- Van Duin, Esther
- Vermeesch, Joris
- Vicari, Stefano
- Vingerhoets, Claudia
- Vorstman, Jacob
- Warren, Steve
- Weinberger, Ronnie
- Weisman, Omri
- Weizman, Abraham
- Zhang, Zhengdong
- Zwick, Michael
2018
Volltextzugriff (PDF)
American journal of human genetics, 2017-10, Vol.101 (4), p.616-622
- Demaerel, Wolfram
- Hestand, Matthew S.
- Vergaelen, Elfi
- Swillen, Ann
- López-Sánchez, Marcos
- Pérez-Jurado, Luis A.
- McDonald-McGinn, Donna M.
- Zackai, Elaine
- Emanuel, Beverly S.
- Morrow, Bernice E.
- Breckpot, Jeroen
- Devriendt, Koenraad
- Vermeesch, Joris R.
- Antshel, Kevin
- Arango, Celso
- Armando, Marco
- Bassett, Anne
- Bearden, Carrie
- Boot, Erik
- Bravo-Sanchez, Marta
- Breetvelt, Elemi
- Busa, Tiffany
- Butcher, Nancy
- Campbell, Linda
- Carmel, Miri
- Chow, Eva
- Crowley, T. Blaine
- Cubells, Joseph
- Cutler, David
- Digilio, Maria Cristina
- Duijff, Sasja
- Eliez, Stephan
- Emanuel, Beverly
- Epstein, Michael
- Evers, Rens
- Fernandez Garcia-Moya, Luis
- Fiksinski, Ania
- Fraguas, David
- Fremont, Wanda
- Fritsch, Rosemarie
- Garcia-Minaur, Sixto
- Golden, Aaron
- Gothelf, Doron
- Guo, Tingwei
- Gur, Ruben
- Gur, Raquel
- Heine-Suner, Damian
- Hestand, Matthew
- Hooper, Stephen
- Kates, Wendy
- Kushan, Leila
- Laorden-Nieto, Alejandra
- Maeder, Johanna
- Marino, Bruno
- Marshall, Christian
- McCabe, Kathryn
- McDonald-McGinn, Donna
- Michaelovosky, Elena
- Morrow, Bernice
- Moss, Edward
- Mulle, Jennifer
- Murphy, Declan
- Murphy, Kieran
- Murphy, Clodagh
- Niarchou, Maria
- Ornstein, Claudia
- Owen, Michael
- Philip, Nicole
- Repetto, Gabriela
- Schneider, Maude
- Shashi, Vandana
- Simon, Tony
- Tassone, Flora
- Unolt, Marta
- van Amelsvoort, Therese
- van den Bree, Marianne
- Van Duin, Esther
- Vermeesch, Joris
- Vicari, Stefano
- Vingerhoets, Claudia
- Vorstman, Jacob
- Warren, Steve
- Weinberger, Ronnie
- Weisman, Omri
- Weizman, Abraham
- Zhang, Zhengdong
- Zwick, Michael
2017
Volltextzugriff (PDF)
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Thema
- 22q11.2 Deletion Syndrome
- 22q11.2ds
- Chromosome Deletion
- Chromosome Inversion
- Digeorge Syndrome
- Digeorge Syndrome - Genetics
- Digeorge Syndrome - Pathology
- Dna Copy Number Variations
- Fiber-Fish
- Genetic Predisposition To Disease
- Genetics & Heredity
- Genomic Disorder
- Homologous Recombination
- Humans
- In Situ Hybridization, Fluorescence - Methods
- Inversion Polymorphism
- Life Sciences & Biomedicine
- Low-Copy Repeats
- Meiosis
- Microdeletion