Results
|
|
161.
|
Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disorders. [electronic resource] by
- Nyström, A-M
- Ekvall, S
- Berglund, E
- Björkqvist, M
- Braathen, G
- Duchen, K
- Enell, H
- Holmberg, E
- Holmlund, U
- Olsson-Engman, M
- Annerén, G
- Bondeson, M-L
Producer: 20080919
In:
Journal of medical genetics vol. 45
Availability: No items available.
|
|
|
162.
|
|
|
|
163.
|
|
|
|
164.
|
Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair. [electronic resource] by
- Ferrero, Giovanni Battista
- Picco, Gabriele
- Baldassarre, Giuseppina
- Flex, Elisabetta
- Isella, Claudio
- Cantarella, Daniela
- Corà, Davide
- Chiesa, Nicoletta
- Crescenzio, Nicoletta
- Timeus, Fabio
- Merla, Giuseppe
- Mazzanti, Laura
- Zampino, Giuseppe
- Rossi, Cesare
- Silengo, Margherita
- Tartaglia, Marco
- Medico, Enzo
Producer: 20120709
In:
Human mutation vol. 33
Availability: No items available.
|
|
|
165.
|
|
|
|
166.
|
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. [electronic resource] by
- Lepri, Francesca
- De Luca, Alessandro
- Stella, Lorenzo
- Rossi, Cesare
- Baldassarre, Giuseppina
- Pantaleoni, Francesca
- Cordeddu, Viviana
- Williams, Bradley J
- Dentici, Maria L
- Caputo, Viviana
- Venanzi, Serenella
- Bonaguro, Michela
- Kavamura, Ines
- Faienza, Maria F
- Pilotta, Alba
- Stanzial, Franco
- Faravelli, Francesca
- Gabrielli, Orazio
- Marino, Bruno
- Neri, Giovanni
- Silengo, Margherita Cirillo
- Ferrero, Giovanni B
- Torrrente, Isabella
- Selicorni, Angelo
- Mazzanti, Laura
- Digilio, Maria C
- Zampino, Giuseppe
- Dallapiccola, Bruno
- Gelb, Bruce D
- Tartaglia, Marco
Producer: 20111014
In:
Human mutation vol. 32
Availability: No items available.
|
|
|
167.
|
|
|
|
168.
|
|
|
|
169.
|
Bisphenol A induces human uterine leiomyoma cell proliferation through membrane-associated ERα36 via nongenomic signaling pathways. [electronic resource] by
- Yu, Linda
- Das, Parikshit
- Vall, Alejandra J
- Yan, Yitang
- Gao, Xioahua
- Sifre, Maria I
- Bortner, Carl D
- Castro, Lysandra
- Kissling, Grace E
- Moore, Alicia B
- Dixon, Darlene
Producer: 20191213
In:
Molecular and cellular endocrinology vol. 484
Availability: No items available.
|
|
|
170.
|
|
|
|
171.
|
Germline gain-of-function mutations in SOS1 cause Noonan syndrome. [electronic resource] by
- Roberts, Amy E
- Araki, Toshiyuki
- Swanson, Kenneth D
- Montgomery, Kate T
- Schiripo, Taryn A
- Joshi, Victoria A
- Li, Li
- Yassin, Yosuf
- Tamburino, Alex M
- Neel, Benjamin G
- Kucherlapati, Raju S
Producer: 20070221
In:
Nature genetics vol. 39
Availability: No items available.
|
|
|
172.
|
Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation. [electronic resource] by
- Chen, Peng-Chieh
- Wakimoto, Hiroko
- Conner, David
- Araki, Toshiyuki
- Yuan, Tao
- Roberts, Amy
- Seidman, Christine E
- Bronson, Roderick
- Neel, Benjamin G
- Seidman, Jonathan G
- Kucherlapati, Raju
Producer: 20110114
In:
The Journal of clinical investigation vol. 120
Availability: No items available.
|
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173.
|
|
|
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174.
|
|
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175.
|
|
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176.
|
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|
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177.
|
|
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178.
|
|
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179.
|
|
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180.
|
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