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                             13 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33 Dai, Xiao-Hua
2008
124 4 p. 423-429
artikel
2 Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci Burdon, Kathryn P.
2008
124 4 p. 379-386
artikel
3 Association between Apolipoprotein E genotype and cerebral palsy is not confirmed in a Caucasian population McMichael, Gai L.
2008
124 4 p. 411-416
artikel
4 Association of amyloid precursor protein-binding protein, family B, member 1 with nicotine dependence in African and European American smokers Chen, Guo-Bo
2008
124 4 p. 393-398
artikel
5 Association of SIRT1 gene variation with visceral obesity Peeters, Armand V.
2008
124 4 p. 431-436
artikel
6 Elof Axel Carlson: Neither gods nor beasts. How science is changing who we think we are Berry, Caroline
2008
124 4 p. 437-438
artikel
7 Human hereditary hearing impairment: mouse models can help to solve the puzzle Vrijens, Karen
2008
124 4 p. 325-348
artikel
8 Identifying modifier genes of monogenic disease: strategies and difficulties Génin, Emmanuelle
2008
124 4 p. 357-368
artikel
9 Osteoporosis: an evolutionary perspective Karasik, David
2008
124 4 p. 349-356
artikel
10 Partial AZFc deletions and duplications: clinical correlates in the Italian population Giachini, Claudia
2008
124 4 p. 399-410
artikel
11 Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation Carvalho, Acácia Fernandes Lacerda de
2008
124 4 p. 387-392
artikel
12 Re-creation of the genetic composition of a founder population Klitz, William
2008
124 4 p. 417-421
artikel
13 The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis Muftuoglu, Meltem
2008
124 4 p. 369-377
artikel
                             13 gevonden resultaten
 
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