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Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated females. [electronic resource] by
- Pöyhönen, Minna H
- Peippo, Maarit M
- Valanne, Leena K
- Kuokkanen, Kirsti E
- Koskela, Susanna M
- Bartsch, Oliver
- Rasi, Sasan
- Wiebe, Glenis J
- Kähkönen, Marketta
- Kääriäinen, Helena A
Producer: 20041110
In:
Clinical dysmorphology vol. 13
Availability: No items available.
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10.
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Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype. [electronic resource] by
- Sawyer, Sarah L
- Tian, Lei
- Kähkönen, Marketta
- Schwartzentruber, Jeremy
- Kircher, Martin
- Majewski, Jacek
- Dyment, David A
- Innes, A Micheil
- Boycott, Kym M
- Moreau, Lisa A
- Moilanen, Jukka S
- Greenberg, Roger A
Producer: 20151022
In:
Cancer discovery vol. 5
Availability: No items available.
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11.
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Primary cutaneous T-cell lymphomas show a deletion or translocation affecting NAV3, the human UNC-53 homologue. [electronic resource] by
- Karenko, Leena
- Hahtola, Sonja
- Päivinen, Suvi
- Karhu, Ritva
- Syrjä, Sanna
- Kähkönen, Marketta
- Nedoszytko, Boguslaw
- Kytölä, Soili
- Zhou, Ying
- Blazevic, Vesna
- Pesonen, Maria
- Nevala, Hanna
- Nupponen, Nina
- Sihto, Harri
- Krebs, Inge
- Poustka, Annemarie
- Roszkiewicz, Jadwiga
- Saksela, Kalle
- Peterson, Pärt
- Visakorpi, Tapio
- Ranki, Annamari
Producer: 20051125
In:
Cancer research vol. 65
Availability: No items available.
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