Detalles de la búsqueda
1.
[Congenital hyperinsulinism--novel insights into etiology, diagnosis and treatment]. / Kongenitalni hiperinzulinizam- -novosti o nastanku, dijagnosticiranju i lijecenju bolesti.
Lijec Vjesn;
134(9-10): 286-92, 2012.
Artículo
en Croata
| MEDLINE | ID: mdl-23297514
2.
Application of microsatellite loci on the chromosome X for rapid prenatal detection of the chromosome X numerical abnormalities.
Croat Med J;
52(3): 392-5, 2011 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-21674836
3.
Cytogenetics of multiple myeloma.
Coll Antropol;
34(1): 41-4, 2010 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-20432732
4.
Pallister Killian syndrome: unusual significant postnatal overgrowth in a girl with otherwise typical presentation.
Coll Antropol;
34(1): 247-50, 2010 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-20437642
5.
Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene.
Coll Antropol;
33(4): 1255-8, 2009 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-20102078
6.
Successful treatment of diffuse large B-cell non-hodgkin lymphoma with modified CHOP (cyclophosphamide/doxorubicin/vincristine/prednisone) chemotherapy and rituximab in a patient with Nijmegen syndrome.
Clin Lymphoma Myeloma;
7(9): 590-3, 2007 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-18186968
7.
Rapid prenatal diagnosis of numerical aberrations of chromosome 21 and 18 by PCR-STR method.
Coll Antropol;
31(3): 859-62, 2007 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-18041400
8.
[Glutaric aciduria type 1: an example of the importance of early detection of so-called cerebral organic aciduria]. / Glutaricka acidurija tipa 1: primjer vaznosti ranog prepoznavanja tzv. cerebralnih organskih acidurija.
Lijec Vjesn;
125(11-12): 312-6, 2003.
Artículo
en Croata
| MEDLINE | ID: mdl-15209027
9.
Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
Croat Med J;
44(4): 477-9, 2003 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-12950153
10.
The first case of the FRAXE form of inherited mental retardation in Croatia.
Eur J Pediatr;
161(2): 112-3, 2002 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-11954745
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