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Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

Clinical genetics, 2017-08, Vol.92 (2), p.166-171

2017

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Monitoring and modeling pesticide fate in surface waters at the catchment scale

Ecological modelling, 2007-11, Vol.209 (1), p.53-64

2007

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Harmonizing Exclusion under the Refugee Convention by Reference to the Evidentiary Standards of International Criminal Law

Journal of international criminal justice, 2014-12, Vol.12 (5), p.1039-1056

Holvoet, M.

2014

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EP-1691 IORT and stray radiation: comparison of 2 commercial linacs

Radiotherapy and oncology, 2019-04, Vol.133, p.S909-S910

2019

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ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism

Clinical genetics, 2004-06, Vol.65 (6), p.503-505

2004

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Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder

Genetic counseling, 2004, Vol.15 (3), p.293

2004

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Extension of the River Water Quality Model No. 1 with the fate of pesticides

Journal of hydroinformatics, 2012-01, Vol.14 (1), p.48-64

2012

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Triplication of distal chromosome 10q

Journal of medical genetics, 1999-03, Vol.36 (3), p.242-245

1999

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The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation

Clinical genetics, 2000-01, Vol.57 (1), p.83-85

2000

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Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1

Journal of medical genetics, 2000-11, Vol.37 (11), p.e34-34

2000

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Partial monosomy 11q and trisomy 12q: variable expression in two siblings

Genetic counseling, 2003, Vol.14 (2), p.155

2003

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Severe mental retardation : distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25 → qter deletion

Clinical genetics, 1998-09, Vol.54 (3), p.224-230

1998

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Further delineation of the KBG syndrome

Genetic counseling, 1998, Vol.9 (3), p.191

1998

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Marden-Walker phenotype: a diagnostic dilemma

Genetic counseling, 1996, Vol.7 (1), p.31

1996

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X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family

European journal of medical genetics, 2005-04, Vol.48 (2), p.145-152

2005

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A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation

Clinical genetics, 1991-06, Vol.39 (6), p.434-441

1991

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A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8

American journal of medical genetics, 1997-09, Vol.74 (5), p.515-520

1997

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Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome

Journal of medical genetics, 1997-05, Vol.34 (5), p.395-399

1997

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Partial DiGeorge syndrome in two patients with a 10p rearrangement

Clinical genetics, 1999-04, Vol.55 (4), p.269-276

1999

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Cri du chat syndrome: Changing phenotype in older patients

American journal of medical genetics, 2000-01, Vol.90 (3), p.203-215

2000

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Follow-up of an adult with Keutel syndrome

American journal of medical genetics, 1999-07, Vol.85 (1), p.82-83

1999

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Severe mental retardation - distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a lOq25→qter deletion

Clinical genetics, 1998-09, Vol.54 (3), p.224-230

1998

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Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: Unusual chromosome 9 variant

American journal of medical genetics, 2000-03, Vol.91 (3), p.192-197

2000

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Physical map of a 1.5Mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint

European journal of human genetics : EJHG, 2000-08, Vol.8 (8), p.561-570

2000

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Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

Monitoring and modeling pesticide fate in surface waters at the catchment scale

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

Harmonizing Exclusion under the Refugee Convention by Reference to the Evidentiary Standards of International Criminal Law

EP-1691 IORT and stray radiation: comparison of 2 commercial linacs

ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder

Extension of the River Water Quality Model No. 1 with the fate of pesticides

Triplication of distal chromosome 10q

The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation

Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1

Partial monosomy 11q and trisomy 12q: variable expression in two siblings

Severe mental retardation : distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25 → qter deletion

Further delineation of the KBG syndrome

Marden-Walker phenotype: a diagnostic dilemma

X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family

A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome

Partial DiGeorge syndrome in two patients with a 10p rearrangement

Cri du chat syndrome: Changing phenotype in older patients

Follow-up of an adult with Keutel syndrome

Severe mental retardation - distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a lOq25→qter deletion

Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: Unusual chromosome 9 variant

Physical map of a 1.5Mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint

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