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Items: 1 to 50 of 84

1.

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

Boot E, Butcher NJ, Udow S, Marras C, Mok KY, Kaneko S, Barrett MJ, Prontera P, Berman BD, Masellis M, Dufournet B, Nguyen K, Charles P, Mutez E, Danaila T, Jacquette A, Colin O, Drapier S, Borg M, Fiksinski AM, Vergaelen E, Swillen A, Vogels A, Plate A, Perandones C, Gasser T, Clerinx K, Bourdain F, Mills K, Williams NM, Wood NW, Booij J, Lang AE, Bassett AS; International Research Group on 22q11.2DS-associated Parkinson's Disease.

Neurology. 2018 May 11. pii: 10.1212/WNL.0000000000005660. doi: 10.1212/WNL.0000000000005660. [Epub ahead of print]

PMID:
29752303
2.

Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.

Swillen A, Moss E, Duijff S.

Am J Med Genet A. 2018 Apr 25. doi: 10.1002/ajmg.a.38709. [Epub ahead of print]

PMID:
29696780
3.

A pilot study on immuno-psychiatry in the 22q11.2 deletion syndrome: A role for Th17 cells in psychosis?

Vergaelen E, Schiweck C, Van Steeland K, Counotte J, Veling W, Swillen A, Drexhage H, Claes S.

Brain Behav Immun. 2018 May;70:88-95. doi: 10.1016/j.bbi.2018.03.022. Epub 2018 Mar 19.

PMID:
29567371
4.

Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.

Guo T, Diacou A, Nomaru H, McDonald-McGinn DM, Hestand M, Demaerel W, Zhang L, Zhao Y, Ujueta F, Shan J, Montagna C, Zheng D, Crowley TB, Kushan-Wells L, Bearden CE, Kates WR, Gothelf D, Schneider M, Eliez S, Breckpot J, Swillen A, Vorstman J, Zackai E, Benavides Gonzalez F, Repetto GM, Emanuel BS, Bassett AS, Vermeesch JR, Marshall CR, Morrow BE; International Chromosome 22q11.2, International 22q11.2 Brain and Behavior Consortia.

Hum Mol Genet. 2018 Apr 1;27(7):1150-1163. doi: 10.1093/hmg/ddy028.

PMID:
29361080
5.

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.

Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, Michaelovsky E, Schneider M, Eliez S, Antonarakis SE, Coleman K, Tomita-Mitchell A, Mitchell ME, Digilio MC, Dallapiccola B, Marino B, Philip N, Busa T, Kushan-Wells L, Bearden CE, Piotrowicz M, Hawuła W, Roberts AE, Tassone F, Simon TJ, van Duin EDA, van Amelsvoort TA, Kates WR, Zackai E, Johnston HR, Cutler DJ, Agopian AJ, Goldmuntz E, Mitchell LE, Wang T, Emanuel BS, Morrow BE; International 22q11.2 Consortium/Brain and Behavior Consortium*.

Circ Cardiovasc Genet. 2017 Oct;10(5). pii: e001690. doi: 10.1161/CIRCGENETICS.116.001690.

6.

Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.

Demaerel W, Hestand MS, Vergaelen E, Swillen A, López-Sánchez M, Pérez-Jurado LA, McDonald-McGinn DM, Zackai E, Emanuel BS, Morrow BE, Breckpot J, Devriendt K, Vermeesch JR; International 22q11.2 Brain and Behavior Consortium.

Am J Hum Genet. 2017 Oct 5;101(4):616-622. doi: 10.1016/j.ajhg.2017.09.002. Epub 2017 Sep 28.

7.

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.

Gur RE, Bassett AS, McDonald-McGinn DM, Bearden CE, Chow E, Emanuel BS, Owen M, Swillen A, Van den Bree M, Vermeesch J, Vorstman JAS, Warren S, Lehner T, Morrow B.

Mol Psychiatry. 2017 Dec;22(12):1664-1672. doi: 10.1038/mp.2017.161. Epub 2017 Aug 1.

PMID:
28761081
8.

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.

Bassett AS, Lowther C, Merico D, Costain G, Chow EWC, van Amelsvoort T, McDonald-McGinn D, Gur RE, Swillen A, Van den Bree M, Murphy K, Gothelf D, Bearden CE, Eliez S, Kates W, Philip N, Sashi V, Campbell L, Vorstman J, Cubells J, Repetto GM, Simon T, Boot E, Heung T, Evers R, Vingerhoets C, van Duin E, Zackai E, Vergaelen E, Devriendt K, Vermeesch JR, Owen M, Murphy C, Michaelovosky E, Kushan L, Schneider M, Fremont W, Busa T, Hooper S, McCabe K, Duijff S, Isaev K, Pellecchia G, Wei J, Gazzellone MJ, Scherer SW, Emanuel BS, Guo T, Morrow BE, Marshall CR; International 22q11.2DS Brain and Behavior Consortium.

Am J Psychiatry. 2017 Nov 1;174(11):1054-1063. doi: 10.1176/appi.ajp.2017.16121417. Epub 2017 Jul 28.

9.

A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome.

Lewyllie A, Roosenboom J, Indencleef K, Claes P, Swillen A, Devriendt K, Carels C, Cadenas De Llano-Pérula M, Willems G, Hens G, Verdonck A.

J Dent Res. 2017 Nov;96(12):1386-1391. doi: 10.1177/0022034517720630. Epub 2017 Jul 21.

PMID:
28732176
10.

High prevalence of fatigue in adults with a 22q11.2 deletion syndrome.

Vergaelen E, Claes S, Kempke S, Swillen A.

Am J Med Genet A. 2017 Apr;173(4):858-867. doi: 10.1002/ajmg.a.38094. Epub 2017 Feb 12.

PMID:
28190295
11.

Numerical magnitude processing impairments in genetic syndromes: a cross-syndrome comparison of Turner and 22q11.2 deletion syndromes.

Brankaer C, Ghesquière P, De Wel A, Swillen A, De Smedt B.

Dev Sci. 2017 Nov;20(6). doi: 10.1111/desc.12458. Epub 2016 Oct 17.

PMID:
27748007
12.

Referential communication abilities in children with 22q11.2 deletion syndrome.

Van Den Heuvel E, ReuterskiöLd C, Solot C, Manders E, Swillen A, Zink I.

Int J Speech Lang Pathol. 2017 Oct;19(5):490-502. doi: 10.1080/17549507.2016.1221456. Epub 2016 Oct 3.

PMID:
27690637
13.

Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome.

Loos E, Verhaert N, Willaert A, Devriendt K, Swillen A, Hermans R, Op de Beeck K, Hens G.

Am J Med Genet A. 2016 Nov;170(11):2975-2983. doi: 10.1002/ajmg.a.37872. Epub 2016 Sep 8.

PMID:
27604838
14.

Developmental trajectories of structural and pragmatic language skills in school-aged children with Williams syndrome.

Van Den Heuvel E, Manders E, Swillen A, Zink I.

J Intellect Disabil Res. 2016 Oct;60(10):903-19. doi: 10.1111/jir.12329. Epub 2016 Aug 22.

PMID:
27546029
15.

A catalog of hemizygous variation in 127 22q11 deletion patients.

Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, Vermeesch JR.

Hum Genome Var. 2016 Jan 14;3:15065. doi: 10.1038/hgv.2015.65. eCollection 2016.

16.

Prevalence and Nature of Hearing Loss in 22q11.2 Deletion Syndrome.

Van Eynde C, Swillen A, Lambeens E, Verhaert N, Desloovere C, Luts H, Poorten VV, Devriendt K, Hens G.

J Speech Lang Hear Res. 2016 Jun 1;59(3):583-9. doi: 10.1044/2015_JSLHR-H-15-0098.

PMID:
27249537
17.

The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome.

Swillen A.

Curr Opin Psychiatry. 2016 Mar;29(2):133-7. doi: 10.1097/YCO.0000000000000231. Review.

18.

Psychotic disorder associated with 22q11.2 duplication syndrome.

van Amelsvoort T, Denayer A, Boermans J, Swillen A.

Psychiatry Res. 2016 Feb 28;236:206-7. doi: 10.1016/j.psychres.2015.12.019. Epub 2015 Dec 17. No abstract available.

PMID:
26763109
19.

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.

Mlynarski EE, Xie M, Taylor D, Sheridan MB, Guo T, Racedo SE, McDonald-McGinn DM, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Philip N, Simon TJ, Roberts AE, Piotrowicz M, Bearden CE, Eliez S, Gothelf D, Coleman K, Kates WR, Devoto M, Zackai E, Heine-Suñer D, Goldmuntz E, Bassett AS, Morrow BE, Emanuel BS; International Chromosome 22q11.2 Consortium.

Hum Genet. 2016 Mar;135(3):273-85. doi: 10.1007/s00439-015-1623-9. Epub 2016 Jan 7.

20.

Developmental trajectories in 22q11.2 deletion.

Swillen A, McDonald-McGinn D.

Am J Med Genet C Semin Med Genet. 2015 Jun;169(2):172-81. doi: 10.1002/ajmg.c.31435. Epub 2015 May 18. Review.

21.

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.

Mlynarski EE, Sheridan MB, Xie M, Guo T, Racedo SE, McDonald-McGinn DM, Gai X, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Philip N, Simon TJ, Roberts AE, Piotrowicz M, Bearden CE, Eliez S, Gothelf D, Coleman K, Kates WR, Devoto M, Zackai E, Heine-Suñer D, Shaikh TH, Bassett AS, Goldmuntz E, Morrow BE, Emanuel BS; International Chromosome 22q11.2 Consortium.

Am J Hum Genet. 2015 May 7;96(5):753-64. doi: 10.1016/j.ajhg.2015.03.007. Epub 2015 Apr 16.

22.

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.

Vorstman JA, Breetvelt EJ, Duijff SN, Eliez S, Schneider M, Jalbrzikowski M, Armando M, Vicari S, Shashi V, Hooper SR, Chow EW, Fung WL, Butcher NJ, Young DA, McDonald-McGinn DM, Vogels A, van Amelsvoort T, Gothelf D, Weinberger R, Weizman A, Klaassen PW, Koops S, Kates WR, Antshel KM, Simon TJ, Ousley OY, Swillen A, Gur RE, Bearden CE, Kahn RS, Bassett AS; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

JAMA Psychiatry. 2015 Apr;72(4):377-85. doi: 10.1001/jamapsychiatry.2014.2671.

23.

3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability.

Vergaelen E, Swillen A, Van Esch H, Claes S, Van Goethem G, Devriendt K.

Eur J Med Genet. 2015 Apr;58(4):244-8. doi: 10.1016/j.ejmg.2015.01.008. Epub 2015 Feb 3.

PMID:
25655469
24.

Practical guidelines for managing adults with 22q11.2 deletion syndrome.

Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, Silversides C, Swillen A, van Amelsvoort T, McDonald-McGinn DM, Bassett AS.

Genet Med. 2015 Aug;17(8):599-609. doi: 10.1038/gim.2014.175. Epub 2015 Jan 8. Review.

25.

22q11.2 deletion syndrome.

McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS.

Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Review.

26.

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, Vorstman J, Duijff SN, Klaassen PW, Swillen A, Gothelf D, Green T, Weizman A, Van Amelsvoort T, Evers L, Boot E, Shashi V, Hooper SR, Bearden CE, Jalbrzikowski M, Armando M, Vicari S, Murphy DG, Ousley O, Campbell LE, Simon TJ, Eliez S; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Am J Psychiatry. 2014 Jun;171(6):627-39. Review.

27.

Presenting symptoms in adults with the 22q11 deletion syndrome.

Vogels A, Schevenels S, Cayenberghs R, Weyts E, Van Buggenhout G, Swillen A, Van Esch H, de Ravel T, Corveleyn P, Devriendt K.

Eur J Med Genet. 2014 Mar;57(4):157-62. doi: 10.1016/j.ejmg.2014.02.008. Epub 2014 Feb 24.

PMID:
24576609
28.
29.

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.

Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M, Higgins AM, Coleman K, Chow C, Jalbrzikowski M, Bearden CE, Bailey A, Vangkilde A, Olsen L, Olesen C, Skovby F, Werge TM, Templin L, Busa T, Philip N, Swillen A, Vermeesch JR, Devriendt K, Schneider M, Dahoun S, Eliez S, Schoch K, Hooper SR, Shashi V, Samanich J, Marion R, van Amelsvoort T, Boot E, Klaassen P, Duijff SN, Vorstman J, Yuen T, Silversides C, Chow E, Bassett A, Frisch A, Weizman A, Gothelf D, Niarchou M, van den Bree M, Owen MJ, Suñer DH, Andreo JR, Armando M, Vicari S, Digilio MC, Auton A, Kates WR, Wang T, Shprintzen RJ, Emanuel BS, Morrow BE.

Am J Hum Genet. 2013 Mar 7;92(3):439-47. doi: 10.1016/j.ajhg.2013.01.018. Epub 2013 Feb 28. Erratum in: Am J Hum Genet. 2013 Apr 4;92(4):637. Jarlbrzkowski, Maria [corrected to Jalbrzikowski, Maria].

30.

Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.

Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon T, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Zackai E, Wang T, Shprintzen R, Emanuel BS, Morrow BE; International Chromosome 22q11.2 Consortium.

Am J Med Genet A. 2012 Nov;158A(11):2781-7. doi: 10.1002/ajmg.a.35512. Epub 2012 Oct 3.

31.

Social phenotypes in genetic syndromes.

Swillen A, de Ravel T, Oliver C.

J Intellect Disabil Res. 2012 Oct;56(10):919-21. doi: 10.1111/j.1365-2788.2012.01620.x. No abstract available.

PMID:
22973833
32.

Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.

Van Campenhout S, Devriendt K, Breckpot J, Frijns JP, Peeters H, Van Buggenhout G, Van Esch H, Maes B, Swillen A.

Genet Couns. 2012;23(2):135-48.

PMID:
22876571
33.

Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills.

Denayer A, Van Esch H, de Ravel T, Frijns JP, Van Buggenhout G, Vogels A, Devriendt K, Geutjens J, Thiry P, Swillen A.

Mol Syndromol. 2012 Jun;3(1):14-20. Epub 2012 May 16.

34.

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.

Guo T, McDonald-McGinn D, Blonska A, Shanske A, Bassett AS, Chow E, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon TJ, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Goldmuntz E, Zackai E, Wang T, Shprintzen R, Emanuel B, Morrow B; International Chromosome 22q11.2 Consortium.

Hum Mutat. 2011 Nov;32(11):1278-89. doi: 10.1002/humu.21568. Epub 2011 Sep 16.

35.

Practical guidelines for managing patients with 22q11.2 deletion syndrome.

Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J; International 22q11.2 Deletion Syndrome Consortium.

J Pediatr. 2011 Aug;159(2):332-9.e1. doi: 10.1016/j.jpeds.2011.02.039. Epub 2011 May 12. No abstract available.

36.

COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome.

Boot E, Booij J, Zinkstok JR, Baas F, Swillen A, Owen MJ, Murphy DG, Murphy KC, Linszen DH, Van Amelsvoort TA.

Synapse. 2011 Sep;65(9):967-70. doi: 10.1002/syn.20932. Epub 2011 Apr 26.

PMID:
21465565
37.

Laterality preference and cognition: cross-syndrome comparison of patients with trisomy 21 (Down), del7q11.23 (Williams-Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) syndromes.

Carlier M, Desplanches AG, Philip N, Stefanini S, Vicari S, Volterra V, Deruelle C, Fisch G, Doyen AL, Swillen A.

Behav Genet. 2011 May;41(3):413-22. doi: 10.1007/s10519-011-9465-2. Epub 2011 Apr 1.

PMID:
21455680
38.

Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls.

Van Aken K, Swillen A, Beirinckx M, Janssens L, Caeyenberghs K, Smits-Engelsman B.

Res Dev Disabil. 2010 May-Jun;31(3):634-41. doi: 10.1016/j.ridd.2010.01.002. Epub 2010 Feb 23.

PMID:
20181458
39.

Kinematic movement strategies in primary school children with 22q11.2 Deletion Syndrome compared to age- and IQ-matched controls during visuo-manual tracking.

Van Aken K, Swillen A, Beirinckx M, Janssens L, Caeyenberghs K, Smits-Engelsman B.

Res Dev Disabil. 2010 May-Jun;31(3):768-76. doi: 10.1016/j.ridd.2010.01.019. Epub 2010 Feb 23.

PMID:
20181457
40.

The motor profile of primary school-age children with a 22q11.2 deletion syndrome (22q11.2DS) and an age- and IQ-matched control group.

Van Aken K, Caeyenberghs K, Smits-Engelsman B, Swillen A.

Child Neuropsychol. 2009 Nov;15(6):532-42. doi: 10.1080/09297040902740678.

PMID:
19280375
41.

Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.

De Smedt B, Swillen A, Verschaffel L, Ghesquière P.

Dev Disabil Res Rev. 2009;15(1):4-10. doi: 10.1002/ddrr.44. Review.

PMID:
19213009
42.

Basic number processing and difficulties in single-digit arithmetic: evidence from Velo-Cardio-Facial Syndrome.

De Smedt B, Reynvoet B, Swillen A, Verschaffel L, Boets B, Ghesquière P.

Cortex. 2009 Feb;45(2):177-88. doi: 10.1016/j.cortex.2007.06.003. Epub 2008 Feb 1.

PMID:
19150519
43.

Cognitive correlates of mathematical disabilities in children with velo-cardio-facial syndrome.

De Smedt B, Swillen A, Devriendt K, Fryns JP, Verschaffel L, Boets B, Ghesquière P.

Genet Couns. 2008;19(1):71-94.

PMID:
18564504
44.

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update.

De Smedt B, Devriendt K, Fryns JP, Vogels A, Gewillig M, Swillen A.

J Intellect Disabil Res. 2007 Sep;51(Pt 9):666-70.

PMID:
17845235
45.

Ocular findings in children with a microdeletion in chromosome 22q11.2.

Casteels I, Casaer P, Gewillig M, Swillen A, Devriendt K.

Eur J Pediatr. 2008 Jul;167(7):751-5. Epub 2007 Aug 18.

PMID:
17704945
46.

Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome).

Van Aken K, De Smedt B, Van Roie A, Gewillig M, Devriendt K, Fryns JP, Simons J, Swillen A.

Dev Med Child Neurol. 2007 Mar;49(3):210-3.

47.

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D.

Hum Mol Genet. 2007 Jan 1;16(1):83-91. Epub 2006 Nov 29.

PMID:
17135275
48.

Mathematical disabilities in young primary school children with velo-cardio-facial syndrome.

De Smedt B, Swillen A, Devriendt K, Fryns JP, Verschaffel L, Ghesquiere P.

Genet Couns. 2006;17(3):259-80.

PMID:
17100194
49.

Mathematical disabilities in children with velo-cardio-facial syndrome.

De Smedt B, Swillen A, Devriendt K, Fryns JP, Verschaffel L, Ghesquière P.

Neuropsychologia. 2007 Mar 14;45(5):885-95. Epub 2006 Oct 17.

PMID:
17049567
50.

Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect.

Swillen A, Feys H, Adriaens T, Nelissen L, Mertens L, Gewillig M, Devriendt K, Fryns JP.

Dev Med Child Neurol. 2005 Dec;47(12):797-802.

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