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Browsing by Author Moeschler, JB
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Showing results 1 to 2 of 2
Title
Author(s)
Issue Date
Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome
Journal:
Journal of Medical Genetics
Tan, TY
Aftimos, S
Worgan, L
Susman, R
Wilson, M
Ghedia, S
Kirk, EP
Love, D
Ronan, A
Darmanian, A
Slavotinek, A
Hogue, J
Moeschler, JB
Ozmore, J
Widmer, R
Savarirayan, R
Peters, G
2009
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome
Journal:
Genetics In Medicine
van der Sluijs, E
Jansen, S
Vergano, SA
Adachi-Fukuda, M
Alanay, T
Alkindy, A
Baban, A
Bayat, A
Beck-Woddl, S
Berry, K
Bijsma, EK
Netzer, C
Ockeloen, CW
Oehl-Jaschkowitz, B
Okamoto, N
Olminkhof, SNM
Orellana, C
Pasquier, L
Pottinger, C
Riehmer, V
Robertson, SP
Roifman, M
Rooryck, C
Ropers, FG
Rosello, M
Ruivenkamp, CAL
Sagiroglu, MS
Sallevelt, SCEH
Sanchis Calvo, A
Simsek-Kipser, PO
Soares, G
Solaeche, L
Mujgan Sonmez, F
Splitt, M
Steenbeek, D
Stegmann, APA
Stumpel, CTRM
Tanabe, S
Uctepe, E
Utine, GE
Veenstra-Knol, HE
Venkateswaran, S
Vilain, C
Vincent-Delorme, C
Vulto-van Silfhout, AT
Wheeler, P
Wilson, GN
Wilson, LC
Wollnik, B
Kosho, T
Wieczorek, D
Eichler, E
Pfundt, R
de Vries, BBA
Clayuton-Smith, J
Santen, GWE
Bok, LA
Brouwer, AFJ
vab der Burgt, I
Campeau, PM
Canham, N
Chrzanowska, K
Chu, WY
Chung, BHY
Dahan, K
De Rademaeker, M
Destree, A
Dudding-Byth, T
Earl, R
Elcioglu, N
Elias, ER
Fagerberg, C
Gardham, A
Gener, B
Gerkes, EH
Grasshoff, U
van Haeringen, A
Heitink, KR
Herkert, JC
den Hollander, NS
Horn, D
Hunt, D
Kant, SG
Kato, M
Kayserili, H
Kersseboom, R
Kilic, E
Krajewska-Walasek, M
Lammers, K
Laulund, LW
Lederer, D
Lees, M
Lopez-Gonzalez, V
Maas, S
Mancini, GMS
Marcelis, C
Martinez, F
Maystadt, I
McGuire, M
McKee, S
Mehta, S
Metcalfe, K
Milunsky, J
Mizuno, S
Moeschler, JB
2018