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Search Results - Veenma, Danielle C. M.
Search Results - Veenma, Danielle C. M.
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Retinol Status of Newborn Infants Is Associated With Congenital Diaphragmatic Hernia
by
BEURSKENS, Leonardus W. J. E
,
TIBBOEL, Dick
,
LINDEMANS, Jan
,
DUVEKOT, Johannes J
,
COHEN-OVERBEEK, Titia E
,
VEENMA, Danielle C. M
,
DE KLEIN, Annelies
,
GREER, John J
,
STEEGERS-THEUNISSEN, Régine P. M
Published in
Pediatrics (Evanston)
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Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys)
by
Dwyer, Bonnie K
,
Veenma, Danielle C M
,
Chang, Kiki
,
Schulman, Howard
,
Van Woerden, Geeske M
Published in
Frontiers in pharmacology
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Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge
by
Brosens, Erwin
,
Peters, Nina C J
,
van Weelden, Kim S
,
Bendixen, Charlotte
,
Brouwer, Rutger W W
,
Sleutels, Frank
,
Bruggenwirth, Hennie T
,
van Ijcken, Wilfred F J
,
Veenma, Danielle C M
,
Otter, Suzan C M Cochius-Den
,
Wijnen, Rene M H
,
Eggink, Alex J
,
van Dooren, Marieke F
,
Reutter, Heiko Martin
,
Rottier, Robbert J
,
Schnater, J Marco
,
Tibboel, Dick
,
de Klein, Annelies
Published in
Frontiers in pediatrics
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Genetic screening of a Dutch population with isolated GH deficiency (IGHD)
by
De Graaff, Laura C. G.
,
Argente, Jesús
,
Veenma, Danielle C. M.
,
Herrebout, Maaike A. C.
,
Friesema, Edith C. H.
,
Uitterlinden, André G.
,
Drent, Madeleine L.
,
Campos-Barros, Ángel
,
Hokken-Koelega, Anita C. S.
Published in
Clinical endocrinology (Oxford)
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Role of CAMK2D in neurodevelopment and associated conditions
by
Rigter, Pomme M.F.
,
de Konink, Charlotte
,
Dunn, Matthew J.
,
Proietti Onori, Martina
,
Humberson, Jennifer B.
,
Thomas, Matthew
,
Barnes, Caitlin
,
Prada, Carlos E.
,
Weaver, K. Nicole
,
Ryan, Thomas D.
,
Caluseriu, Oana
,
Conway, Jennifer
,
Calamaro, Emily
,
Fong, Chin-To
,
Wuyts, Wim
,
Meuwissen, Marije
,
Hordijk, Eva
,
Jonkers, Carsten N.
,
Anderson, Lucas
,
Yuseinova, Berfin
,
Polonia, Sarah
,
Beysen, Diane
,
Stark, Zornitza
,
Savva, Elena
,
Poulton, Cathryn
,
McKenzie, Fiona
,
Bhoj, Elizabeth
,
Bupp, Caleb P.
,
Bézieau, Stéphane
,
Mercier, Sandra
,
Blevins, Amy
,
Wentzensen, Ingrid M.
,
Xia, Fan
,
Rosenfeld, Jill A.
,
Hsieh, Tzung-Chien
,
Krawitz, Peter M.
,
Elbracht, Miriam
,
Veenma, Danielle C.M.
,
Schulman, Howard
,
Stratton, Margaret M.
,
Küry, Sébastien
,
van Woerden, Geeske M.
Published in
American journal of human genetics
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5q35 duplication syndrome: Narrowing the critical region on the distal side and further evidence of intrafamilial variability and expression
by
Lugt, Neeltje Margreth
,
Weerts, Marjolein J. A.
,
Veenma, Danielle C. M.
,
Lincke, Carsten R.
,
Gischler, Saskia J.
,
Alders, Marielle
,
Ierland, Yvette
Published in
American journal of medical genetics. Part A
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Incomplete spinal cord injury following minor trauma in two siblings with spondylocostal dysostis type 6
by
van der Vlis, Tim A. M. Bouwens
,
Boeykens, Annegien
,
Jacobs, Elke
,
Veenma, Danielle C. M.
,
Thompson, Dominic N. P.
,
Bannink, N.
,
Joor, Fleur
,
Renkens, Jeroen
,
Rutges, Joost P. H. J.
,
Harhangi, Biswadjiet S.
,
Spoor, Jochem K. H.
Published in
Spine deformity
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Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys)
by
Dwyer, Bonnie K
,
Veenma, Danielle C M
,
Chang, Kiki
,
Schulman, Howard
,
Van Woerden, Geeske M
Published in
Frontiers in pharmacology
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5q35 duplication syndrome: Narrowing the critical region on the distal side and further evidence of intrafamilial variability and expression
by
van der Lugt, Neeltje Margreth
,
Weerts, Marjolein J A
,
Veenma, Danielle C M
,
Lincke, Carsten R
,
Gischler, Saskia J
,
Alders, Marielle
,
van Ierland, Yvette
Published in
American journal of medical genetics. Part A
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Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?
by
Gaillard, Linda
,
Goverde, Anne
,
van den Bosch, Quincy C C
,
Jehee, Fernanda S
,
Brosens, Erwin
,
Veenma, Danielle
,
Magielsen, Frank
,
de Klein, Annelies
,
Mathijssen, Irene M J
,
van Dooren, Marieke F
Published in
Frontiers in pediatrics
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Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity
by
Costain, Gregory
,
Walker, Susan
,
Marano, Maria
,
Veenma, Danielle
,
Snell, Meaghan
,
Curtis, Meredith
,
Luca, Stephanie
,
Buera, Jason
,
Arje, Danielle
,
Reuter, Miriam S
,
Thiruvahindrapuram, Bhooma
,
Trost, Brett
,
Sung, Wilson W L
,
Yuen, Ryan K C
,
Chitayat, David
,
Mendoza-Londono, Roberto
,
Stavropoulos, D James
,
Scherer, Stephen W
,
Marshall, Christian R
,
Cohn, Ronald D
,
Cohen, Eyal
,
Orkin, Julia
,
Meyn, M Stephen
,
Hayeems, Robin Z
Published in
JAMA network open
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Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?
by
Gaillard, Linda
,
Goverde, Anne
,
van den Bosch, Quincy C C
,
Jehee, Fernanda S
,
Brosens, Erwin
,
Veenma, Danielle
,
Magielsen, Frank
,
de Klein, Annelies
,
Mathijssen, Irene M J
,
van Dooren, Marieke F
Published in
Frontiers in pediatrics
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