Søgeresultater - Alida C. Knegt
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1
Selective chromosome analysis in couples with two or more miscarriages: case-control study af Maureen Franssen, Johanna C. Korevaar, N. J. Leschot, Patrick M. Bossuyt, Alida C. Knegt, Klasien B.J. Gerssen‐Schoorl, Carine Wouters, Kerstin Hansson, Ron Hochstenbach, K. Madan, Fulco van der Veen, Mariëtte Goddijn
Udgivet 2005Artigo -
2
Genetic basis of alpha‐aminoadipic and alpha‐ketoadipic aciduria af Jacob Hagen, Heleen te Brinke, Ronald J. A. Wanders, Alida C. Knegt, Esmée Oussoren, A. Jeannette M. Hoogeboom, George J. G. Ruijter, Daniel M. Becker, Karl Otfried Schwab, Ingo Franke, Marinus Durán, Hans R. Waterham, Jörn Oliver Sass, Sander M. Houten
Udgivet 2015Artigo -
3
Genetic basis of hyperlysinemia af Sander M. Houten, Heleen te Brinke, Simone Denis, Jos P.N. Ruiter, Alida C. Knegt, J. B. de Klerk, Persephone Augoustides‐Savvopoulou, Johannes Häberle, Matthias R. Baumgartner, Turgay Coşkun, Johannes Zschocke, Jörn Oliver Sass, Bwee Tien Poll‐The, Ronald J. A. Wanders, Marinus Durán
Udgivet 2013Artigo -
4
The prevalence of genetic diagnoses in fetuses with severe congenital heart defects af A. van Nisselrooij, Malou A. Lugthart, Sally‐Ann B. Clur, Ingeborg H. Linskens, Eva Pajkrt, Lukas Rammeloo, Lieke Rozendaal, Nico A. Blom, J. M. M. van Lith, Alida C. Knegt, Mariëtte J.V. Hoffer, Emmelien Aten, Gijs W.E. Santen, Monique C. Haak
Udgivet 2020Artigo -
5
Embryonic stem cell-like cells derived from adult human testis af Sefika C Mizrak, J.V. Chikhovskaya, Hooman Sadri‐Ardekani, Silke F. van Daalen, Cindy M. Korver, Suzanne Hovingh, Hermien L. Roepers‐Gajadien, Ángel Raya, Kees Fluiter, T.M. De Reijke, Jean de la Rosette, Alida C. Knegt, Juan Carlos Izpisúa Belmonte, Fulco van der Veen, Dirk G. de Rooij, Sjoerd Repping, Ans M. M. van Pelt
Udgivet 2009Artigo
Søgeredskaber:
Relaterede emner
Biology
Genetics
Gene
Medicine
Mutation
Internal medicine
Missense mutation
Pregnancy
Abortion
Adult stem cell
Alpha (finance)
Amino acid substitution
Amniotic epithelial cells
Aneuploidy
Atrioventricular Septal Defect
Bioinformatics
Cell biology
Chromosome
Cohort
Construct validity
Disease
Down syndrome
Embryonic stem cell
Exome sequencing
Family history
Fetal echocardiography
Fetus
Frameshift mutation
G alpha subunit
Gene duplication