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Prediction of alternative isoforms from exon expression levels in RNA-Seq experiments. [electronic resource] by
- Richard, Hugues
- Schulz, Marcel H
- Sultan, Marc
- Nürnberger, Asja
- Schrinner, Sabine
- Balzereit, Daniela
- Dagand, Emilie
- Rasche, Axel
- Lehrach, Hans
- Vingron, Martin
- Haas, Stefan A
- Yaspo, Marie-Laure
Producer: 20100622
In:
Nucleic acids research vol. 38
Availability: No items available.
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15.
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Functional analysis and identification of cis-regulatory elements of human chromosome 21 gene promoters. [electronic resource] by
- Warnatz, Hans-Jörg
- Querfurth, Robert
- Guerasimova, Anna
- Cheng, Xi
- Haas, Stefan A
- Hufton, Andrew L
- Manke, Thomas
- Vanhecke, Dominique
- Nietfeld, Wilfried
- Vingron, Martin
- Janitz, Michal
- Lehrach, Hans
- Yaspo, Marie-Laure
Producer: 20101102
In:
Nucleic acids research vol. 38
Availability: No items available.
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16.
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Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing. [electronic resource] by
- Hu, Hao
- Wrogemann, Klaus
- Kalscheuer, Vera
- Tzschach, Andreas
- Richard, Hugues
- Haas, Stefan A
- Menzel, Corinna
- Bienek, Melanie
- Froyen, Guy
- Raynaud, Martine
- Van Bokhoven, Hans
- Chelly, Jamel
- Ropers, Hilger
- Chen, Wei
Producer: 20110714
In:
The HUGO journal vol. 3
Availability: No items available.
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17.
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Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing. [electronic resource] by
- Hu, Hao
- Wrogemann, Klaus
- Kalscheuer, Vera
- Tzschach, Andreas
- Richard, Hugues
- Haas, Stefan A
- Menzel, Corinna
- Bienek, Melanie
- Froyen, Guy
- Raynaud, Martine
- Van Bokhoven, Hans
- Chelly, Jamel
- Ropers, Hilger
- Chen, Wei
Producer: 20111110
In:
The HUGO journal vol. 3
Availability: No items available.
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18.
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Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep. [electronic resource] by
- Hecht, Jochen
- Kuhl, Heiner
- Haas, Stefan A
- Bauer, Sebastian
- Poustka, Albert J
- Lienau, Jasmin
- Schell, Hanna
- Stiege, Asita C
- Seitz, Volkhard
- Reinhardt, Richard
- Duda, Georg N
- Mundlos, Stefan
- Robinson, Peter N
Producer: 20061127
In:
BMC genomics vol. 7
Availability: No items available.
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19.
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Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. [electronic resource] by
- Lesca, Gaetan
- Moizard, Marie-Pierre
- Bussy, Gerald
- Boggio, Dominique
- Hu, Hao
- Haas, Stefan A
- Ropers, Hans-Hilger
- Kalscheuer, Vera M
- Des Portes, Vincent
- Labalme, Audrey
- Sanlaville, Damien
- Edery, Patrick
- Raynaud, Martine
- Lespinasse, James
Producer: 20140702
In:
American journal of medical genetics. Part A vol. 161A
Availability: No items available.
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20.
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X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes. [electronic resource] by
- Philips, Anju K
- Sirén, Auli
- Avela, Kristiina
- Somer, Mirja
- Peippo, Maarit
- Ahvenainen, Minna
- Doagu, Fatma
- Arvio, Maria
- Kääriäinen, Helena
- Van Esch, Hilde
- Froyen, Guy
- Haas, Stefan A
- Hu, Hao
- Kalscheuer, Vera M
- Järvelä, Irma
Producer: 20140926
In:
Orphanet journal of rare diseases vol. 9
Availability: No items available.
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