N. Clusellas

发表

New Bactericide Orthodonthic Archwire: NiTi with Silver Nanoparticles

F. Gil, Andreu Puigdollers, Eduardo Espinar-Escalona, 2020, Metals.

Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis

Y. Shen, M. Obón, A. Soler, 2013, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

MLPA: a prenatal diagnostic tool for the study of congenital heart defects?

Aurora Sánchez, A. Soler, I. Mademont-Soler, 2012, Gene.

Identification of 14 novel mutations in DHCR7 causing the Smith‐Lemli‐Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and Italy

P. Clayton, G. Utermann, R. Kelley, 2005, Human mutation.

Comparison of Lingual and Buccal Orthodontic Therapy on Microbial Parameters and Periodontal Status

Andreu Puigdollers, M. Franch, A. Walter, 2019 .

FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t(5;8)(q33;q13)

J. Egozcue, F. Vidal, J. Blanco, 1999, Cytogenetic and Genome Research.

Prenatal cytogenetic diagnosis in Spain: analysis and evaluation of the results obtained from amniotic fluid samples during the last decade.

Aurora Sánchez, A. Soler, I. Mademont-Soler, 2011, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocation

I. Madrigal, Aurora Sánchez, A. Borrell, 2009, American journal of medical genetics. Part A.

Subtelomeric MLPA: is it really useful in prenatal diagnosis?

I. Madrigal, Aurora Sánchez, J. Bruguera, 2010, Prenatal diagnosis.

Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues.

M. Milá, Aurora Sánchez, V. Catalá, 2010, European journal of medical genetics.

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations

X. Estivill, P. Talmud, D. Labuda, 2007, Journal of Medical Genetics.

Assessment of QF-PCR as the first approach in prenatal diagnosis.

C. Badenas, M. Milá, L. Rodriguez-Revenga, 2010, The Journal of molecular diagnostics : JMD.

DE NOVO INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 2 IN A MALFORMED NEWBORN WITH A KARYOTYPE: 46, XY, del(2)(q12q14)

X. Carbonell, N. Clusellas, J. Antich, 1983, Acta paediatrica Scandinavica.

Feasibility of molecular prenatal diagnosis of glutaric aciduria type I in chorionic villi

A. Ribes, E. Christensen, M. Vilaseca, 1998, Journal of Inherited Metabolic Disease.

Structural chromosome rearrangements in prenatal diagnosis: results from a Spanish database.

L. Nonell, R. A. de la Chica, N. Clusellas, 2015, European journal of obstetrics, gynecology, and reproductive biology.

Bimaxillary Surgery with Maxillary Segmentation and Lingual Orthodontics

Andreu Puigdollers, A. Arcas, N. Clusellas, 2018 .

Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability

C. Badenas, Aurora Sánchez, Irene Mademont, 2012, American journal of medical genetics. Part A.