Results
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4601.
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4602.
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4603.
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4604.
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4605.
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Inactivation of the Na-Cl co-transporter (NCC) gene is associated with high BMD through both renal and bone mechanisms: analysis of patients with Gitelman syndrome and Ncc null mice. [electronic resource] by
- Nicolet-Barousse, Laurence
- Blanchard, Anne
- Roux, Christian
- Pietri, Laurence
- Bloch-Faure, May
- Kolta, Sami
- Chappard, Christine
- Geoffroy, Valérie
- Morieux, Caroline
- Jeunemaitre, Xavier
- Shull, Gary E
- Meneton, Pierre
- Paillard, Michel
- Houillier, Pascal
- De Vernejoul, Marie-Christine
Producer: 20050819
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 20
Availability: No items available.
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4606.
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4607.
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4609.
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4610.
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An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism. [electronic resource] by
- Bowl, Michael R
- Nesbit, M Andrew
- Harding, Brian
- Levy, Elaine
- Jefferson, Andrew
- Volpi, Emanuela
- Rizzoti, Karine
- Lovell-Badge, Robin
- Schlessinger, David
- Whyte, Michael P
- Thakker, Rajesh V
Producer: 20051212
In:
The Journal of clinical investigation vol. 115
Availability: No items available.
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4611.
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Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome. [electronic resource] by
- Parvari, Ruti
- Hershkovitz, Eli
- Grossman, Nili
- Gorodischer, Rafael
- Loeys, Bart
- Zecic, Alexandra
- Mortier, Geert
- Gregory, Simon
- Sharony, Reuven
- Kambouris, Marios
- Sakati, Nadia
- Meyer, Brian F
- Al Aqeel, Aida I
- Al Humaidan, Abdul Karim
- Al Zanhrani, Fatma
- Al Swaid, Abdulrahman
- Al Othman, Johara
- Diaz, George A
- Weiner, Rory
- Khan, K Tahseen S
- Gordon, Ronald
- Gelb, Bruce D
Producer: 20021224
In:
Nature genetics vol. 32
Availability: No items available.
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4612.
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4613.
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Surgery for Neck Recurrence of Differentiated Thyroid Cancer: Outcomes and Risk Factors. [electronic resource] by
- Lamartina, Livia
- Borget, Isabelle
- Mirghani, Haitham
- Al Ghuzlan, Abir
- Berdelou, Amandine
- Bidault, François
- Deandreis, Désirée
- Baudin, Eric
- Travagli, Jean-Paul
- Schlumberger, Martin
- Hartl, Dana M
- Leboulleux, Sophie
Producer: 20170612
In:
The Journal of clinical endocrinology and metabolism vol. 102
Availability: No items available.
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4614.
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4615.
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4617.
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4618.
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4619.
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4620.
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Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome. [electronic resource] by
- Nesbit, M Andrew
- Bowl, Michael R
- Harding, Brian
- Ali, Asif
- Ayala, Alejandro
- Crowe, Carol
- Dobbie, Angus
- Hampson, Geeta
- Holdaway, Ian
- Levine, Michael A
- McWilliams, Robert
- Rigden, Susan
- Sampson, Julian
- Williams, Andrew J
- Thakker, Rajesh V
Producer: 20040630
In:
The Journal of biological chemistry vol. 279
Availability: No items available.
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