Centrum Menselijke Erfelijkheid
29 titels · 2008–2016 · 1 imprint
Medische biologieNon-fictie informatief/professioneel algemeenSpecialistische geneeskunde: algemeenDieetboekenMedische en socio-medische wetenschappenGezondheidswetenschappen
Over deze uitgeverij
Centrum Menselijke Erfelijkheid staat met 29 titels in de boekenbase en publiceerde tussen 2008–2016. Er valt één imprint onder deze uitgeverij. Het fonds valt vooral onder medische biologie, non-fictie informatief/professioneel algemeen, specialistische geneeskunde: algemeen.
Recent verschenen
Discovery of novel genes for intellectual disability and multiple congenital anomalies in the next generation sequencing era
Mala Isrie
Discovery of novel genes for intellectual disability and multiple congenital anomalies in the next generation sequencing era
Mala Isrie
Paperback · 2016
Cognitie en gedrag in neurofibromatose type 1 en Legius syndroom
Ellen Plasschaert
Cognitie en gedrag in neurofibromatose type 1 en Legius syndroom
Ellen Plasschaert
Paperback · 2015
Chromosomal microarrays for prenatal diagnosis and genetic variants in congenital diaphragmatic Hernia
Paul Daniel Brady
Chromosomal microarrays for prenatal diagnosis and genetic variants in congenital diaphragmatic Hernia
Paul Daniel Brady
Paperback · 2014
Cytogenetic and genomic assessment of selected lymphoproliferative disorders
Natalie Put
Cytogenetic and genomic assessment of selected lymphoproliferative disorders
Natalie Put
Paperback · 2012
Genetics of brain malformations
Elyes Chabchoub
Genetics of brain malformations
Elyes Chabchoub
Paperback · 2012
Copy Number Variation in Congenital Heart Defects
Jeroen Breckpot
Copy Number Variation in Congenital Heart Defects
Jeroen Breckpot
Paperback · 2011
The molecular dissection of contiguous gene syndromes with a focus on 4p16 deletion syndrome
F. Hannes
The molecular dissection of contiguous gene syndromes with a focus on 4p16 deletion syndrome
F. Hannes
Paperback · 2011
Molecular and functional characterization of a new neuro-cardio-facial-cutaneous syndrome: Legius syndrome
Hilde Brems
Molecular and functional characterization of a new neuro-cardio-facial-cutaneous syndrome: Legius syndrome
Hilde Brems
Paperback · 2010
Naar een lichter en gezonder gewicht
Veerle Govers
Naar een lichter en gezonder gewicht
Veerle Govers
Losbladig · 2010
Naar een lichter en gezonder gewicht
Veerle Govers
Naar een lichter en gezonder gewicht
Veerle Govers
Hardback · 2010
Single cell array analysis of cleavage stage embryos
Evelyne Vanneste
Single cell array analysis of cleavage stage embryos
Evelyne Vanneste
Paperback · 2010
Identification and characterization of new lymphoma-associated genetic aberrations involving protein tyrosine kinase loci
Katrien Van Roosbroeck
Identification and characterization of new lymphoma-associated genetic aberrations involving protein tyrosine kinase loci
Katrien Van Roosbroeck
Paperback · 2010
PDGF receptors as therapeutic targets in sarcomas
Barbara Dewaele
PDGF receptors as therapeutic targets in sarcomas
Barbara Dewaele
Paperback · 2010
Genetic studies in developmental skeletal and limb defects
Boyan Ivanov Dimitrov
Genetic studies in developmental skeletal and limb defects
Boyan Ivanov Dimitrov
Paperback · 2010
The role of copy number variations in the etiology of congenital ocular malformations
Irina Balikova
The role of copy number variations in the etiology of congenital ocular malformations
Irina Balikova
Paperback · 2010
Genetic Diagnosis in Mental Retardation
T. de Ravel de l'Argentiare
Genetic Diagnosis in Mental Retardation
T. de Ravel de l'Argentiare
Paperback · 2009
Improving our insight in the genetic origin of congenital heart defects using array comparative genome hybridization
B. Thienpont
Improving our insight in the genetic origin of congenital heart defects using array comparative genome hybridization
B. Thienpont
Paperback · 2009
Microarray comparative genome hybridization in mental retardation / congenital malformations
N. Maas
Microarray comparative genome hybridization in mental retardation / congenital malformations
N. Maas
Paperback · 2008
Behavioral phenotupe in velo-cardio-facial sybdrome
A. Swillen
Behavioral phenotupe in velo-cardio-facial sybdrome
A. Swillen
Paperback
A systematic genetic-etiological survey in a Dutch population of institutionalised mentally retarded patients
G. Van Buggenhout
A systematic genetic-etiological survey in a Dutch population of institutionalised mentally retarded patients
G. Van Buggenhout
Paperback
Prenatal diognosis of fetal malformations and chromosomal anomolie & multidisciplinary approach
I. Witters
Prenatal diognosis of fetal malformations and chromosomal anomolie & multidisciplinary approach
I. Witters
Hardback
Plag 1 involvement in cellular transformation and embryonic
K. Hensen
Plag 1 involvement in cellular transformation and embryonic
K. Hensen
Paperback
The behavioural phenotype in two dynamic mutation disorders
J. Steyaert
The behavioural phenotype in two dynamic mutation disorders
J. Steyaert
Paperback
Clinical and molecular genetics of mental retardation from phenotype to genotype to phenotype
S.G.M. Frints
Clinical and molecular genetics of mental retardation from phenotype to genotype to phenotype
S.G.M. Frints
Paperback
Psychosis in the Prader-Willi Syndrome
A. Vogels
Psychosis in the Prader-Willi Syndrome
A. Vogels
Paperback
Positional cloning of four candidate genes for autism
D. Castermans
Positional cloning of four candidate genes for autism
D. Castermans
Paperback
PA26is a novel gene required for left-right asymetry
Hagar Peeters
PA26is a novel gene required for left-right asymetry
Hagar Peeters
Paperback
A psychological perspective on genetic testing for hereditary cancers
E. Claes
A psychological perspective on genetic testing for hereditary cancers
E. Claes
Hardback
Gata 3 haplionsufficiency causes hypoparathyroidism sensorineural deafness and renal anomalies
H. van Esch
Gata 3 haplionsufficiency causes hypoparathyroidism sensorineural deafness and renal anomalies
H. van Esch
Paperback
Imprints
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