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 |