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                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Announcement 2006
 69 2 p. 198
 artikel
2 Corrigendum 2006
 69 2 p. 197
 artikel
3 Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosis Nisselle, AE
 2006
 69 2 p. 163-170
 artikel
4 Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families Gerdes, A-M
 2006
 69 2 p. 171-178
 artikel
5 Familial carpal tunnel syndrome: further evidence for a genetic contribution 2006
 69 2 p. 179-182
 artikel
6 In Memoriam 2006
 69 2 p. 194-196
 artikel
7 Jewels in the rough – the study of non-coding genomic sequences as a conduit to understanding human disease Pouladi, MA
 2006
 69 2 p. 118-119
 artikel
8 Molecular characterization of a balanced chromosome translocation in psoriasis vulgaris 2006
 69 2 p. 189-193
 artikel
9 Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene Feldman, M
 2006
 69 2 p. 135-144
 artikel
10 Multiple gynecologic tumors as rare associated phenotypes of FAP/Gardner syndrome in a family with the novel germline mutation in the APC gene 2006
 69 2 p. 183-186
 artikel
11 Prevalence of HFE C282Y and H63D in Jewish populations and clinical implications of H63D homozygosity Matas, M
 2006
 69 2 p. 155-162
 artikel
12 15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH Koochek, M
 2006
 69 2 p. 124-134
 artikel
13 Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies Krabchi, K
 2006
 69 2 p. 145-154
 artikel
14 Two clinical forms of glycogen-storage disease type II in two generations of the same family 2006
 69 2 p. 187-188
 artikel
15 Ultrasound detection of placental insufficiency in women with ‘unexplained’ abnormal maternal serum screening results Whittle, W
 2006
 69 2 p. 97-104
 artikel
16 Vesicoureteric reflux and renal malformations: a developmental problem Murawski, IJ
 2006
 69 2 p. 105-117
 artikel
                             16 gevonden resultaten
 
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