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2961.
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Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations. [electronic resource] by
- Unger, Sheila
- Böhm, Detlef
- Kaiser, Frank J
- Kaulfuss, Silke
- Borozdin, Wiktor
- Buiting, Karin
- Burfeind, Peter
- Böhm, Johann
- Barrionuevo, Francisco
- Craig, Alexander
- Borowski, Kristi
- Keppler-Noreuil, Kim
- Schmitt-Mechelke, Thomas
- Steiner, Bernhard
- Bartholdi, Deborah
- Lemke, Johannes
- Mortier, Geert
- Sandford, Richard
- Zabel, Bernhard
- Superti-Furga, Andrea
- Kohlhase, Jürgen
Producer: 20080402
In:
Nature genetics vol. 40
Availability: No items available.
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2971.
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2972.
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2973.
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Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract. [electronic resource] by
- Dong, Shuangshuang
- Wang, Chunyan
- Li, Xueping
- Shen, Qian
- Fu, Xiaoyi
- Wu, Mingyan
- Song, Chengcheng
- Yang, Nan
- Wu, Yanhua
- Wang, Hongyan
- Jin, Li
- Xu, Hong
- Zhang, Feng
Producer: 20190326
In:
Molecular genetics and genomics : MGG vol. 294
Availability: No items available.
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2974.
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2975.
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Urogenital Abnormalities in Adenosine Deaminase Deficiency. [electronic resource] by
- Pajno, Roberta
- Pacillo, Lucia
- Recupero, Salvatore
- Cicalese, Maria P
- Ferrua, Francesca
- Barzaghi, Federica
- Ricci, Silvia
- Marzollo, Antonio
- Pecorelli, Silvia
- Azzari, Chiara
- Finocchi, Andrea
- Cancrini, Caterina
- Di Matteo, Gigliola
- Russo, Gianni
- Alfano, Massimo
- Lesma, Arianna
- Salonia, Andrea
- Adams, Stuart
- Booth, Claire
- Aiuti, Alessandro
Producer: 20210806
In:
Journal of clinical immunology vol. 40
Availability: No items available.
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2978.
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