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                             11 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A de novo 17q21.2 duplication in a boy with developmental delay and dysmorphic features Poirsier-Violle, Céline
2013
56 4 p. 226-228
3 p.
artikel
2 Allan–Herndon–Dudley syndrome (AHDS) in two consecutive generations caused by a missense MCT8 gene mutation. Phenotypic variability with the presence of normal serum T3 levels Boccone, Loredana
2013
56 4 p. 207-210
4 p.
artikel
3 A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate Izzo, Giselle
2013
56 4 p. 222-225
4 p.
artikel
4 A small de novo 16q24.1 duplication in a woman with severe clinical features Quéméner-Redon, Sylvia
2013
56 4 p. 211-215
5 p.
artikel
5 Exon 2 duplication of the MID1 gene in a patient with a mild phenotype of Opitz G/BBB syndrome Hüning, Irina
2013
56 4 p. 188-191
4 p.
artikel
6 Mutation analysis of ATP7B gene in Turkish Wilson disease patients: Identification of five novel mutations Simsek Papur, Ozlenen
2013
56 4 p. 175-179
5 p.
artikel
7 Non-mosaic uniparental trisomy 16 presenting with asplenia syndrome and placental abruption: A case report and literature review Su, Mei-Tsz
2013
56 4 p. 197-201
5 p.
artikel
8 Patient with Dup(5)(q35.2-q35.3) reciprocal to the common Sotos syndrome deletion and review of the literature Žilina, Olga
2013
56 4 p. 202-206
5 p.
artikel
9 3q26.33–3q27.2 microdeletion: A new microdeletion syndrome? Mandrile, Giorgia
2013
56 4 p. 216-221
6 p.
artikel
10 The effect of the cleidocranial dysplasia-related novel 1116_1119insC mutation in the RUNX2 gene on the biological function of mesenchymal cells Ding, Bofu
2013
56 4 p. 180-187
8 p.
artikel
11 To know or not to know, disclosure of a newborn carrier screening test result for cystic fibrosis Vernooij-van Langen, Annette M.M.
2013
56 4 p. 192-196
5 p.
artikel
                             11 gevonden resultaten
 
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