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Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

European journal of human genetics : EJHG, 1998-06, Vol.6 (3), p.194-200

1998

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Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa

Human reproduction (Oxford), 1997-04, Vol.12 (4), p.752-754

1997

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Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

European journal of human genetics : EJHG, 1998-05, Vol.6 (3), p.194-200

1998

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ARE DOWN SYNDROME FETUSES DETECTED THROUGH MATERNAL SERUM SCREENING SIMILAR TO THOSE REMAINING UNDETECTED?

Prenatal diagnosis, 1996-05, Vol.16 (5), p.437-442

1996

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Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome

Clinical genetics, 1985-01, Vol.27 (1), p.92-96

1985

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Partial trisomy 11q due to paternal t(11q;18p); further delineation of the clinical picture

Clinical genetics, 1984-03, Vol.25 (3), p.295-299

1984

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Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)

Clinical genetics, 1984-09, Vol.26 (3), p.209-215

1984

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Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion

Clinical genetics, 1984-10, Vol.26 (4), p.379-382

1984

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A third case of de novo partial trisomy 4p

Journal of medical genetics, 1989-05, Vol.26 (5), p.344-345

1989

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Interstitial deletion of the long arm of chromosome 11

Journal of medical genetics, 1985-06, Vol.22 (3), p.224-226

1985

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Two cases with different deletions of the long arm of chromosome 7

Journal of medical genetics, 1979-04, Vol.16 (2), p.151-154

1979

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Cytogenetic investigations in volunteers ingesting inorganic lead

International archives of occupational and environmental health, 1976-12, Vol.38 (2), p.145-148

1976

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On the use of distribution-functions to describe and classify chromosome density-profiles

Computers in biology and medicine, 1979, Vol.9 (1), p.11-20

1979

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A system for automatic metaphase finding and semi-automatic chromosome analysis

Microscopica acta. Supplement, 1979 (3), p.213

1979

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Metaphase location and chromosome identification by means of the Quantimet 720D. A semi-automatic approach

Microscopica acta. Supplement, 1977 (1), p.105

1977

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18q− and 18q+ mosaicism in a mentally retarded boy

American journal of medical genetics, 1994-11, Vol.53 (3), p.296-299

1994

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The Dutch uniform multicenter registration system for genetic disorders and malformation syndromes

American journal of medical genetics, 1997-06, Vol.70 (4), p.444-447

1997

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Establishment of the origin of a porcine cell line by chromosome banding techniques and scanning

The Journal of laboratory and clinical medicine, 1976-12, Vol.88 (6), p.965

1976

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Automated selection of metaphase cells by quality

Cytometry (New York, N.Y.), 1981-05, Vol.1 (6), p.363-368

1981

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Congenital glaucoma in a child with partial lq duplication and 9p deletion

Ophthalmic genetics, 1992, Vol.13 (3), p.165-170

1992

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Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?

Human genetics, 1977-01, Vol.38 (1), p.7-13

1977

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Partial trisomy 10q: a recognizable syndrome

Human genetics, 1979-01, Vol.46 (1), p.29-40

1979

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Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome

Human genetics, 1978-01, Vol.40 (2), p.135-147

1978

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Direct giemsa-banding pattern analysis of human chromosomes by means of a television microdensitometer: The Quantimet 720 D

Humangenetik, 1974-06, Vol.22 (2), p.167-170

1974

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Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure

The New England journal of medicine, 2020-10, Vol.383 (15), p.1413-1424

2020

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Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

ARE DOWN SYNDROME FETUSES DETECTED THROUGH MATERNAL SERUM SCREENING SIMILAR TO THOSE REMAINING UNDETECTED?

Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome

Partial trisomy 11q due to paternal t(11q;18p); further delineation of the clinical picture

Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)

Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion

A third case of de novo partial trisomy 4p

Interstitial deletion of the long arm of chromosome 11

Two cases with different deletions of the long arm of chromosome 7

Cytogenetic investigations in volunteers ingesting inorganic lead

On the use of distribution-functions to describe and classify chromosome density-profiles

A system for automatic metaphase finding and semi-automatic chromosome analysis

Metaphase location and chromosome identification by means of the Quantimet 720D. A semi-automatic approach

18q− and 18q+ mosaicism in a mentally retarded boy

The Dutch uniform multicenter registration system for genetic disorders and malformation syndromes

Establishment of the origin of a porcine cell line by chromosome banding techniques and scanning

Automated selection of metaphase cells by quality

Congenital glaucoma in a child with partial lq duplication and 9p deletion

Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?

Partial trisomy 10q: a recognizable syndrome

Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome

Direct giemsa-banding pattern analysis of human chromosomes by means of a television microdensitometer: The Quantimet 720 D

Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure

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