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Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts. [electronic resource] by
- Vogelaar, Ingrid P
- Figueiredo, Joana
- van Rooij, Iris A L M
- Simões-Correia, Joana
- van der Post, Rachel S
- Melo, Soraia
- Seruca, Raquel
- Carels, Carine E L
- Ligtenberg, Marjolijn J L
- Hoogerbrugge, Nicoline
Producer: 20130722
In:
Human molecular genetics vol. 22
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Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias. [electronic resource] by
- Söderhäll, Cilla
- Körberg, Izabella Baranowska
- Thai, Hanh T T
- Cao, Jia
- Chen, Yougen
- Zhang, Xufeng
- Shulu, Zu
- van der Zanden, Loes F M
- van Rooij, Iris A L M
- Frisén, Louise
- Roeleveld, Nel
- Markljung, Ellen
- Kockum, Ingrid
- Nordenskjöld, Agneta
Producer: 20151215
In:
European journal of human genetics : EJHG vol. 23
Availability: No items available.
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33.
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First results of a European multi-center registry of patients with anorectal malformations. [electronic resource] by
- de Blaauw, Ivo
- Wijers, Charlotte H W
- Schmiedeke, Eberhard
- Holland-Cunz, Stefan
- Gamba, Piergiorgio
- Marcelis, Carlo L M
- Reutter, Heiko
- Aminoff, Dalia
- Schipper, Muriel
- Schwarzer, Nicole
- Grasshoff-Derr, Sabine
- Midrio, Paola
- Jenetzky, Ekkehart
- van Rooij, Iris A L M
Producer: 20140821
In:
Journal of pediatric surgery vol. 48
Availability: No items available.
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34.
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Uncontrolled maternal chronic respiratory diseases in pregnancy: A new potential risk factor suggested to be associated with anorectal malformations in offspring. [electronic resource] by
- van de Putte, Romy
- de Blaauw, Ivo
- Boenink, Rianne
- Reijers, Monique H E
- Broens, Paul M A
- Sloots, Cornelius E J
- van Heijst, Arno F J
- van Gelder, Marleen M H J
- Roeleveld, Nel
- van Rooij, Iris A L M
Producer: 20191202
In:
Birth defects research vol. 111
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35.
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Previous miscarriages and GLI2 are associated with anorectal malformations in offspring. [electronic resource] by
- van de Putte, Romy
- Wijers, Charlotte H W
- de Blaauw, Ivo
- Marcelis, Carlo L M
- Sloots, Cornelius E J
- Brooks, Alice S
- Broens, Paul M A
- Roeleveld, Nel
- van der Zanden, Loes F M
- van Rooij, Iris A L M
Producer: 20180222
In:
Human reproduction (Oxford, England) vol. 32
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36.
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Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract: A case-control study. [electronic resource] by
- Groen In 't Woud, Sander
- Renkema, Kirsten Y
- Schreuder, Michiel F
- Wijers, Charlotte H W
- van der Zanden, Loes F M
- Knoers, Nine V A M
- Feitz, Wout F J
- Bongers, Ernie M H F
- Roeleveld, Nel
- van Rooij, Iris A L M
Producer: 20171012
In:
Birth defects research. Part A, Clinical and molecular teratology vol. 106
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37.
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Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias. [electronic resource] by
- van de Putte, Romy
- Wijers, Charlotte H W
- de Blaauw, Ivo
- Feitz, Wout F J
- Marcelis, Carlo L M
- Hakobjan, Marina
- Sloots, Cornelius E J
- van Bever, Yolande
- Brunner, Han G
- Roeleveld, Nel
- van Rooij, Iris A L M
- van der Zanden, Loes F M
Producer: 20160223
In:
European journal of pediatrics vol. 174
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38.
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No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformations. [electronic resource] by
- Wijers, Charlotte H W
- de Blaauw, Ivo
- Zwink, Nadine
- Draaken, Markus
- van der Zanden, Loes F M
- Brunner, Han G
- Brooks, Alice S
- Hofstra, Robert M
- Sloots, Cornelius E J
- Broens, Paul M A
- Wijnen, Marc H
- Ludwig, Michael
- Jenetzky, Ekkehart
- Reutter, Heiko
- Marcelis, Carlo L M
- Roeleveld, Nel
- van Rooij, Iris A L M
Producer: 20150202
In:
Birth defects research. Part A, Clinical and molecular teratology vol. 100
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39.
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Genome-wide association analyses identify variants in developmental genes associated with hypospadias. [electronic resource] by
- Geller, Frank
- Feenstra, Bjarke
- Carstensen, Lisbeth
- Pers, Tune H
- van Rooij, Iris A L M
- Körberg, Izabella Baranowska
- Choudhry, Shweta
- Karjalainen, Juha M
- Schnack, Tine H
- Hollegaard, Mads V
- Feitz, Wout F J
- Roeleveld, Nel
- Hougaard, David M
- Hirschhorn, Joel N
- Franke, Lude
- Baskin, Laurence S
- Nordenskjöld, Agneta
- van der Zanden, Loes F M
- Melbye, Mads
Producer: 20150115
In:
Nature genetics vol. 46
Availability: No items available.
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40.
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De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations. [electronic resource] by
- Dworschak, Gabriel C
- Draaken, Markus
- Marcelis, Carlo
- de Blaauw, Ivo
- Pfundt, Rolph
- van Rooij, Iris A L M
- Bartels, Enrika
- Hilger, Alina
- Jenetzky, Ekkehart
- Schmiedeke, Eberhard
- Grasshoff-Derr, Sabine
- Schmidt, Dominik
- Märzheuser, Stefanie
- Hosie, Stuart
- Weih, Sandra
- Holland-Cunz, Stefan
- Palta, Markus
- Leonhardt, Johannes
- Schäfer, Mattias
- Kujath, Christina
- Rissmann, Anke
- Nöthen, Markus M
- Zwink, Nadine
- Ludwig, Michael
- Reutter, Heiko
Producer: 20140702
In:
American journal of medical genetics. Part A vol. 161A
Availability: No items available.
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