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7821.
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Rare A2ML1 variants confer susceptibility to otitis media. [electronic resource] by
- Santos-Cortez, Regie Lyn P
- Chiong, Charlotte M
- Reyes-Quintos, Ma Rina T
- Tantoco, Ma Leah C
- Wang, Xin
- Acharya, Anushree
- Abbe, Izoduwa
- Giese, Arnaud P
- Smith, Joshua D
- Allen, E Kaitlynn
- Li, Biao
- Cutiongco-de la Paz, Eva Maria
- Garcia, Marieflor Cristy
- Llanes, Erasmo Gonzalo D V
- Labra, Patrick John
- Gloria-Cruz, Teresa Luisa I
- Chan, Abner L
- Wang, Gao T
- Daly, Kathleen A
- Shendure, Jay
- Bamshad, Michael J
- Nickerson, Deborah A
- Patel, Janak A
- Riazuddin, Saima
- Sale, Michele M
- Chonmaitree, Tasnee
- Ahmed, Zubair M
- Abes, Generoso T
- Leal, Suzanne M
Producer: 20151026
In:
Nature genetics vol. 47
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7822.
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7823.
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Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity. [electronic resource] by
- De Rocker, Nina
- Vergult, Sarah
- Koolen, David
- Jacobs, Eva
- Hoischen, Alexander
- Zeesman, Susan
- Bang, Birgitte
- Béna, Frédérique
- Bockaert, Nele
- Bongers, Ernie M
- de Ravel, Thomy
- Devriendt, Koenraad
- Giglio, Sabrina
- Faivre, Laurence
- Joss, Shelagh
- Maas, Saskia
- Marle, Nathalie
- Novara, Francesca
- Nowaczyk, Malgorzata J M
- Peeters, Hilde
- Polstra, Abeltje
- Roelens, Filip
- Rosenberg, Carla
- Thevenon, Julien
- Tümer, Zeynep
- Vanhauwaert, Suzanne
- Varvagiannis, Konstantinos
- Willaert, Andy
- Willemsen, Marjolein
- Willems, Marjolaine
- Zuffardi, Orsetta
- Coucke, Paul
- Speleman, Frank
- Eichler, Evan E
- Kleefstra, Tjitske
- Menten, Björn
Producer: 20160224
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 17
Availability: No items available.
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7824.
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Differential impact of allelic ratio and insertion site in FLT3-ITD-positive AML with respect to allogeneic transplantation. [electronic resource] by
- Schlenk, Richard F
- Kayser, Sabine
- Bullinger, Lars
- Kobbe, Guido
- Casper, Jochen
- Ringhoffer, Mark
- Held, Gerhard
- Brossart, Peter
- Lübbert, Michael
- Salih, Helmut R
- Kindler, Thomas
- Horst, Heinz A
- Wulf, Gerald
- Nachbaur, David
- Götze, Katharina
- Lamparter, Alexander
- Paschka, Peter
- Gaidzik, Verena I
- Teleanu, Veronica
- Späth, Daniela
- Benner, Axel
- Krauter, Jürgen
- Ganser, Arnold
- Döhner, Hartmut
- Döhner, Konstanze
Producer: 20150223
In:
Blood vol. 124
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7825.
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7826.
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Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes. [electronic resource] by
- Woodbury-Smith, Marc
- Paterson, Andrew D
- Thiruvahindrapduram, Bhooma
- Lionel, Anath C
- Marshall, Christian R
- Merico, Daniele
- Fernandez, Bridget A
- Duku, Eric
- Sutcliffe, James S
- O'Conner, Irene
- Chrysler, Christina
- Thompson, Ann
- Kellam, Barbara
- Tammimies, Kristiina
- Walker, Susan
- Yuen, Ryan K C
- Uddin, Mohammed
- Howe, Jennifer L
- Parlier, Morgan
- Whitten, Kathy
- Szatmari, Peter
- Vieland, Veronica J
- Piven, Joseph
- Scherer, Stephen W
Producer: 20150417
In:
Human genetics vol. 134
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7827.
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Whole genome duplication and enrichment of metal cation transporters revealed by de novo genome sequencing of extremely halotolerant black yeast Hortaea werneckii. [electronic resource] by
- Lenassi, Metka
- Gostinčar, Cene
- Jackman, Shaun
- Turk, Martina
- Sadowski, Ivan
- Nislow, Corey
- Jones, Steven
- Birol, Inanc
- Cimerman, Nina Gunde
- Plemenitaš, Ana
Producer: 20140408
In:
PloS one vol. 8
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7828.
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7829.
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7830.
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7831.
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Co-Circulation of 72bp Duplication Group A and 60bp Duplication Group B Respiratory Syncytial Virus (RSV) Strains in Riyadh, Saudi Arabia during 2014. [electronic resource] by
- Ahmed, Anwar
- Haider, Shakir H
- Parveen, Shama
- Arshad, Mohammed
- Alsenaidy, Hytham A
- Baaboud, Alawi Omar
- Mobaireek, Khalid Fahad
- AlSaadi, Muslim Mohammed
- Alsenaidy, Abdulrahman M
- Sullender, Wayne
Producer: 20170710
In:
PloS one vol. 11
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7832.
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7833.
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7834.
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7835.
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Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American families. [electronic resource] by
- Romero, Pablo T
- Donoso, Rodrigo
- López, Pamela
- Miranda, Ana
- Rodríguez, Leandro
- Chrzanowsky, Dominique
- Asenjo, Maria S
- Burgos, Gonzalo
- Villegas, Pablo
- Desir, Julie
- Moya, Graciela
- Herrera, Luisa M
Producer: 20200313
In:
Ophthalmic genetics vol. 40
Availability: No items available.
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7836.
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Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish Community. [electronic resource] by
- Tester, David J
- Bombei, Hannah M
- Fitzgerald, Kristi K
- Giudicessi, John R
- Pitel, Beth A
- Thorland, Erik C
- Russell, Barbara G
- Hamrick, Samantha K
- Kim, C S John
- Haglund-Turnquist, Carla M
- Johnsrude, Christopher L
- Atkins, Dianne L
- Ochoa Nunez, Luis A
- Law, Ian
- Temple, Joel
- Ackerman, Michael J
Producer: 20210111
In:
JAMA cardiology vol. 5
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7837.
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