Results
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31041.
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31042.
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A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas. [electronic resource] by
- Maier-Woelfle, Margarete
- Brändle, Michael
- Komminoth, Paul
- Saremaslani, Parvin
- Schmid, Sonja
- Locher, Tamara
- Heitz, Philipp U
- Krull, Ina
- Galeazzi, Renato L
- Schmid, Christoph
- Perren, Aurel
Producer: 20040211
In:
The Journal of clinical endocrinology and metabolism vol. 89
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31043.
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Microsatellite DNA alterations of gastrointestinal stromal tumors are predictive for outcome. [electronic resource] by
- Schurr, Paulus
- Wolter, Stefan
- Kaifi, Jussuf
- Reichelt, Uta
- Kleinhans, Helge
- Wachowiak, Robin
- Yekebas, Emre
- Strate, Tim
- Kalinin, Viacheslav
- Simon, Ronald
- Sauter, Guido
- Schaefer, Hansjoerg
- Izbicki, Jakob
Producer: 20071130
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 12
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31044.
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31045.
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31046.
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31047.
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31048.
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31049.
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31050.
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31051.
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31052.
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The genetic structure of Pacific Islanders. [electronic resource] by
- Friedlaender, Jonathan S
- Friedlaender, Françoise R
- Reed, Floyd A
- Kidd, Kenneth K
- Kidd, Judith R
- Chambers, Geoffrey K
- Lea, Rodney A
- Loo, Jun-Hun
- Koki, George
- Hodgson, Jason A
- Merriwether, D Andrew
- Weber, James L
Producer: 20080226
In:
PLoS genetics vol. 4
Availability: No items available.
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31053.
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Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. [electronic resource] by
- Brookes, K J
- Xu, X
- Anney, R
- Franke, B
- Zhou, K
- Chen, Wai
- Banaschewski, T
- Buitelaar, J
- Ebstein, R
- Eisenberg, J
- Gill, M
- Miranda, A
- Oades, R D
- Roeyers, H
- Rothenberger, A
- Sergeant, J
- Sonuga-Barke, E
- Steinhausen, H-C
- Taylor, E
- Faraone, S V
- Asherson, P
Producer: 20090106
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 147B
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31054.
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Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract. [electronic resource] by
- Cohen, David
- Bar-Yosef, Udy
- Levy, Jaime
- Gradstein, Libe
- Belfair, Nadav
- Ofir, Rivka
- Joshua, Sarah
- Lifshitz, Tova
- Carmi, Rivka
- Birk, Ohad S
Producer: 20070613
In:
Investigative ophthalmology & visual science vol. 48
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31055.
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31056.
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Preimplantation genetic diagnosis for fetal neonatal alloimmune thrombocytopenia due to antihuman platelet antigen maternal antibodies. [electronic resource] by
- Altarescu, Gheona
- Eldar-Geva, T
- Geva, T Eldar
- Grisaru-Granovsky, Sorina
- Bonstein, Lilach
- Miskin, Hagit
- Varshver, Irit
- Margalioth, Ehud J
- Levy-Lahad, Ephrat
- Renbaum, Paul
Producer: 20120611
In:
Obstetrics and gynecology vol. 119
Availability: No items available.
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31057.
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A c.3216_3217delGA mutation in AGL gene in Tunisian patients with a glycogen storage disease type III: evidence of a founder effect. [electronic resource] by
- Mili, A
- Ben Charfeddine, I
- Amara, A
- Mamaï, O
- Adala, L
- Ben Lazreg, T
- Bouguila, J
- Saad, A
- Limem, K
- Gribaa, M
Producer: 20130412
In:
Clinical genetics vol. 82
Availability: No items available.
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31059.
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31060.
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