J M Scheres|G F Merkx - JoVE Visualize

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Tijdschrift Voor Kindergeneeskunde|August 1, 1986

[Down's syndrome in the Netherlands]T W Hustinx, J M Scheres, J P Geraedts, et al.

Human Genetics|July 12, 1978

15/17 translocation in acute promyelocytic leukaemiaJ M Scheres, T W Hustinx, G A de Vaan, et al.

Human Reproduction (Oxford, England)|November 6, 1998

One normal child and a chromosomally balanced/normal twin after intracytoplasmic sperm injection in a male with a de-novo t(Y;16) translocationJ C Giltay, C H Tiemessen, W G van Inzen, et al.

Cancer|October 1, 1983

Malignant histiocytosis. Clinical and cytogenetic studies in a newborn and a childT J Schouten, T W Hustinx, J M Scheres, et al.

Human Genetics|September 1, 1994

ICF syndrome: a new case and review of the literatureD F Smeets, U Moog, C M Weemaes, et al.

Mutation Research|February 1, 1983

Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage SyndromeR D Taalman, N G Jaspers, J M Scheres, et al.

Cancer Genetics and Cytogenetics|November 1, 1985

Translocation 1;7 in hematologic disorders: a brief review of 22 casesJ M Scheres, T W Hustinx, J P Geraedts, et al.

Journal of Medical Genetics|October 1, 1992

Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parentC J Van Der Burgt, G F Merkx, A H Janssen, et al.

Cancer Genetics and Cytogenetics|November 24, 1999

Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1qJ M Scheres, J M de Pater, P Stoutenbeek, et al.

Human Genetics|June 19, 1979

Karyotype instability with multiple 7/14 and 7/7 rearrangementsT W Hustinx, J M Scheres, C M Weemaes, et al.

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Showing results (21-30 of 56) with videos related to

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Tijdschrift Voor Kindergeneeskunde|August 1, 1986

[Down's syndrome in the Netherlands]T W Hustinx, J M Scheres, J P Geraedts, et al.

Human Genetics|July 12, 1978

15/17 translocation in acute promyelocytic leukaemiaJ M Scheres, T W Hustinx, G A de Vaan, et al.

Human Reproduction (Oxford, England)|November 6, 1998

One normal child and a chromosomally balanced/normal twin after intracytoplasmic sperm injection in a male with a de-novo t(Y;16) translocationJ C Giltay, C H Tiemessen, W G van Inzen, et al.

Cancer|October 1, 1983

Malignant histiocytosis. Clinical and cytogenetic studies in a newborn and a childT J Schouten, T W Hustinx, J M Scheres, et al.

Human Genetics|September 1, 1994

ICF syndrome: a new case and review of the literatureD F Smeets, U Moog, C M Weemaes, et al.

Mutation Research|February 1, 1983

Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage SyndromeR D Taalman, N G Jaspers, J M Scheres, et al.

Cancer Genetics and Cytogenetics|November 1, 1985

Translocation 1;7 in hematologic disorders: a brief review of 22 casesJ M Scheres, T W Hustinx, J P Geraedts, et al.

Journal of Medical Genetics|October 1, 1992

Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parentC J Van Der Burgt, G F Merkx, A H Janssen, et al.

Cancer Genetics and Cytogenetics|November 24, 1999

Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1qJ M Scheres, J M de Pater, P Stoutenbeek, et al.

Human Genetics|June 19, 1979

Karyotype instability with multiple 7/14 and 7/7 rearrangementsT W Hustinx, J M Scheres, C M Weemaes, et al.

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