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01286naa a2200325 i 4500 |
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NSK01000948394 |
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HR-ZaNSK |
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20161124114809.0 |
| 007 |
ta |
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161115s2014 ci | |0|| ||eng |
| 035 |
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|a (HR-ZaNSK)000948394
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|a HR-ZaNSK
|b hrv
|c HR-ZaNSK
|e ppiak
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0 |
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|a eng
|b hrv
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|a croatica
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| 044 |
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|a ci
|c hr
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| 080 |
1 |
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|a 616
|2 MRF 2011.
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| 100 |
1 |
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|a Katavić, Matej
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| 245 |
1 |
0 |
|a Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene /
|c Matej Katavić, Monika Kukuruzović, Maša Malenica, Sara Seneca, Ljerka Cvitanović-Šojat.
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| 504 |
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|a Bibliografija: 9 jed.
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| 504 |
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|a Sažetak
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| 653 |
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0 |
|a Rettov sindrom
|a Neurorazvojni poremećaji
|a Neurološki poremećaji
|a Epilepsija
|a Genetska analiza
|a Mutacije
|a Dijete
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| 653 |
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6 |
|a Prikaz slučaja
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| 700 |
1 |
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|a Kukuruzović, Monika
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| 700 |
1 |
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|a Malenica, Maša
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| 700 |
1 |
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|a Seneca, Sara
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| 700 |
1 |
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|a Cvitanović-Šojat, Ljerka
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| 773 |
0 |
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|t Paediatria Croatica
|x 1330-1403
|g 58 (2014), 4 ; str. 283-285
|w nsk.(HR-ZaNSK)000022369
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| 981 |
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|b B09/14
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| 998 |
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|a gtao1611
|a bokd1611
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| 856 |
4 |
2 |
|u http://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=210018
|y Elektronička verzija članka
|