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Characterization of a chromosome 8‐derived minute marker chromosome using microdissection and FISH in a boy with growth retardation

American journal of medical genetics, 2003-04, Vol.118A (3), p.274-278

2003

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Familial partial trisomy 8p without dysmorphic features and only mild mental retardation

Journal of medical genetics, 1995-10, Vol.32 (10), p.792-795

1995

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Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication

Clinical genetics, 1994-12, Vol.46 (6), p.423-429

1994

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An outpatient nursing nutritional intervention to prehabilitate undernourished patients planned for surgery: A multicentre, cluster-randomised pilot study

Clinical nutrition (Edinburgh, Scotland), 2020-08, Vol.39 (8), p.2420-2427

2020

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Using intervention mapping to develop an outpatient nursing nutritional intervention to improve nutritional status in undernourished patients planned for surgery

BMC health services research, 2020-02, Vol.20 (1), p.152-152, Article 152

2020

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Partial trisomy and monosomy 8p due to inversion duplication

Clinical genetics, 1994-04, Vol.45 (4), p.203-207

1994

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Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers

American journal of medical genetics. Part A, 2004-10, Vol.130A (2), p.128-133

2004

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Deletion of chromosome region 18q21.1 → 18q21.3 in a patient without clinical features of the 18q‐ phenotype

American journal of medical genetics, 2003-06, Vol.119A (3), p.356-359

2003

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Paracentric inversion inv(11) (q21q23) in the Netherlands

Human genetics, 1990-06, Vol.85 (1), p.15-20

1990

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Intrachromosomal insertion translocation resulting in duplication of chromosome band Yq11.2 in two fertile brothers

American journal of medical genetics. Part A, 2003-04, Vol.118A (3), p.287-289

2003

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Duplication of chromosome region (16)(p11.2 → p12.1) in a mother and daughter with mild mental retardation

American journal of medical genetics, 2002-04, Vol.109 (2), p.149-153

2002

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On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms

Clinical genetics, 1987-12, Vol.32 (6), p.409-413

1987

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Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3)

Journal of medical genetics, 1998-07, Vol.35 (7), p.604-608

1998

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The frequency and types of resident relocations in Dutch nursing homes: a nationwide cohort study of electronic health record data

European geriatric medicine, 2024-10

2024

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Teaching and learning thinking skills

1999

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Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH

Journal of medical genetics, 1996-07, Vol.33 (7), p.562-566

1996

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Application of micro-FISH to delineate deletions

Cytogenetic and genome research, 1996-01, Vol.75 (2-3), p.167-171

1996

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Clinical and Chromosome Studies of Three Patients with Smith‐Magenis Syndrome

Developmental medicine and child neurology, 1991-04, Vol.33 (4), p.343-347

1991

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Duplication of chromosome region 8p23.1 → p23.3: A benign variant?

American journal of medical genetics, 2000-03, Vol.91 (1), p.18-21

2000

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Rate of recombination of chromosomes 21 in parents of children with Down syndrome

Clinical genetics, 1990-06, Vol.37 (6), p.463-469

1990

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Clinical and chromosome studies of three patients withy Smith-Magenis syndrome

Developmental medicine and child neurology, 1991, Vol.33 (4), p.343-347

1991

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De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISH

American journal of medical genetics, 2001-04, Vol.100 (1), p.56-61

2001

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De novo "pure" partial trisomy (6)(p22.1→pter) in a chromosome 15 with an enlarged satellite, identified by microdissection

American journal of medical genetics, 2001-02, Vol.99 (1), p.48-53

2001

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Complex Chromosome 9, 20, and 22 Rearrangements in Acute Lymphoblastic Leukemia with Duplication of BCR and ABL Sequences

Cancer genetics and cytogenetics, 2000-01, Vol.116 (2), p.119-123

2000

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Characterization of a partial trisomy 16q with FISH. Report of a patient and review of the literature

Annales de génétique, 1999, Vol.42 (2), p.101

1999

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Characterization of a chromosome 8‐derived minute marker chromosome using microdissection and FISH in a boy with growth retardation

Familial partial trisomy 8p without dysmorphic features and only mild mental retardation

Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication

An outpatient nursing nutritional intervention to prehabilitate undernourished patients planned for surgery: A multicentre, cluster-randomised pilot study

Using intervention mapping to develop an outpatient nursing nutritional intervention to improve nutritional status in undernourished patients planned for surgery

Partial trisomy and monosomy 8p due to inversion duplication

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers

Deletion of chromosome region 18q21.1 → 18q21.3 in a patient without clinical features of the 18q‐ phenotype

Paracentric inversion inv(11) (q21q23) in the Netherlands

Intrachromosomal insertion translocation resulting in duplication of chromosome band Yq11.2 in two fertile brothers

Duplication of chromosome region (16)(p11.2 → p12.1) in a mother and daughter with mild mental retardation

On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms

Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3)

The frequency and types of resident relocations in Dutch nursing homes: a nationwide cohort study of electronic health record data

Teaching and learning thinking skills

Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH

Application of micro-FISH to delineate deletions

Clinical and Chromosome Studies of Three Patients with Smith‐Magenis Syndrome

Duplication of chromosome region 8p23.1 → p23.3: A benign variant?

Rate of recombination of chromosomes 21 in parents of children with Down syndrome

Clinical and chromosome studies of three patients withy Smith-Magenis syndrome

De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISH

De novo "pure" partial trisomy (6)(p22.1→pter) in a chromosome 15 with an enlarged satellite, identified by microdissection

Complex Chromosome 9, 20, and 22 Rearrangements in Acute Lymphoblastic Leukemia with Duplication of BCR and ABL Sequences

Characterization of a partial trisomy 16q with FISH. Report of a patient and review of the literature

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