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Decreased ACKR3 (CXCR7) function causes oculomotor synkinesis in mice and humans. [electronic resource] by
- Whitman, Mary C
- Miyake, Noriko
- Nguyen, Elaine H
- Bell, Jessica L
- Matos Ruiz, Paola M
- Chan, Wai-Man
- Di Gioia, Silvio Alessandro
- Mukherjee, Nisha
- Barry, Brenda J
- Bosley, T M
- Khan, Arif O
- Engle, Elizabeth C
Producer: 20200309
In:
Human molecular genetics vol. 28
Availability: No items available.
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Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes. [electronic resource] by
- Costa-Barbosa, Flavia Amanda
- Balasubramanian, Ravikumar
- Keefe, Kimberly W
- Shaw, Natalie D
- Al-Tassan, Nada
- Plummer, Lacey
- Dwyer, Andrew A
- Buck, Cassandra L
- Choi, Jin-Ho
- Seminara, Stephanie B
- Quinton, Richard
- Monies, Dorota
- Meyer, Brian
- Hall, Janet E
- Pitteloud, Nelly
- Crowley, William F
Producer: 20130705
In:
The Journal of clinical endocrinology and metabolism vol. 98
Availability: No items available.
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