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Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype. [electronic resource] by
- Ojeda, Diego
- Lakhal, Besma
- Fonseca, Dora Janneth
- Braham, Rim
- Landolsi, Hanène
- Mateus, Heidi Eliana
- Restrepo, Carlos Martín
- Elghezal, Hatem
- Saâd, Ali
- Laissue, Paul
Producer: 20110826
In:
Fertility and sterility vol. 95
Availability: No items available.
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16.
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Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7. [electronic resource] by
- Reddy, Ramesh
- Akoury, Elie
- Phuong Nguyen, Ngoc Minh
- Abdul-Rahman, Omar A
- Dery, Christine
- Gupta, Neerja
- Daley, William P
- Ao, Asangla
- Landolsi, Hanene
- Ann Fisher, Rosemary
- Touitou, Isabelle
- Slim, Rima
Producer: 20140324
In:
European journal of human genetics : EJHG vol. 21
Availability: No items available.
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17.
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CITED2 mutations potentially cause idiopathic premature ovarian failure. [electronic resource] by
- Fonseca, Dora Janeth
- Ojeda, Diego
- Lakhal, Besma
- Braham, Rim
- Eggers, Stefanie
- Turbitt, Erin
- White, Stefan
- Grover, Sonia
- Warne, Garry
- Zacharin, Margaret
- Nevin Lam, Alexandra
- Landolsi, Hanène
- Elghezal, Hatem
- Saâd, Ali
- Restrepo, Carlos Martín
- Fellous, Marc
- Sinclair, Andrew
- Koopman, Peter
- Laissue, Paul
Producer: 20130306
In:
Translational research : the journal of laboratory and clinical medicine vol. 160
Availability: No items available.
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18.
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Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte. [electronic resource] by
- Parry, David A
- Logan, Clare V
- Hayward, Bruce E
- Shires, Michael
- Landolsi, Hanène
- Diggle, Christine
- Carr, Ian
- Rittore, Cécile
- Touitou, Isabelle
- Philibert, Laurent
- Fisher, Rosemary A
- Fallahian, Masoumeh
- Huntriss, John D
- Picton, Helen M
- Malik, Saghira
- Taylor, Graham R
- Johnson, Colin A
- Bonthron, David T
- Sheridan, Eamonn G
Producer: 20111122
In:
American journal of human genetics vol. 89
Availability: No items available.
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