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Estimation of 3-D Ocean Wave Spectra from Spotlight Sar Data During Saxon-Fpn

[Proceedings] IGARSS '92 International Geoscience and Remote Sensing Symposium, 1992, Vol.2, p.1097-1099

1992

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Classification Of Forested Terrain Using Multifrequency, Polarimetric Sap, Data

10th Annual International Symposium on Geoscience and Remote Sensing, 1990, p.2401-2401

1990

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Establishment and characterization of an uveal‐melanoma cell line

International journal of cancer, 1995-07, Vol.62 (2), p.155-161

1995

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Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature

American journal of medical genetics, 2003-10, Vol.122A (2), p.168-173

2003

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Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3

Journal of medical genetics, 1997-07, Vol.34 (7), p.569-572

1997

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Effect of subcutaneously administered human recombinant erythropoietin on erythropoiesis in patients with myelodysplasia

British journal of haematology, 1991-08, Vol.78 (4), p.488-493

1991

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Effect of Mast Cell Growth Factor (c-kit ligand) on Clonogenic Leukemic Precursor Cells

Blood, 1992-08, Vol.80 (3), p.750-757

1992

Volltextzugriff (PDF)

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCE IN SITU HYBRIDIZATION

Prenatal diagnosis, 1997-02, Vol.17 (2), p.173-179

1997

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Amniocentesis before 14 completed weeks as an alternative to transabdominal chorionic villus sampling: a controlled trial with infant follow-up

Prenatal diagnosis, 1998-05, Vol.18 (5), p.465-475

1998

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46,XY del(18) (q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome

Clinical genetics, 1993-02, Vol.43 (2), p.76-78

1993

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Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male

Journal of medical genetics, 1989-05, Vol.26 (5), p.330-333

1989

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Chromosome abnormalities in a patient with acquired immunodeficiency syndrome (AIDS) and Burkitt lymphoma-leukemia

Leukemia, 1990-06, Vol.4 (6), p.445-447

1990

Volltextzugriff (PDF)

Monosomy 8p: an easily overlooked syndrome

Journal of medical genetics, 1986-04, Vol.23 (2), p.153-154

1986

Volltextzugriff (PDF)

A patient with an interstitial deletion of the short arm of chromosome 6

Clinical genetics, 1988-02, Vol.33 (2), p.95-101

1988

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LETTER TO THE EDITOR. YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME 18 HETERMORPHISMS?

Prenatal diagnosis, 1997-06, Vol.17 (6), p.585-586

1997

Volltextzugriff (PDF)

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3

Journal of medical genetics, 1997-07, Vol.34 (7), p.569-572

1997

Volltextzugriff (PDF)

Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis: A Case Report and Review of the Literature

Cancer genetics and cytogenetics, 1999-11, Vol.115 (1), p.11-18

1999

Volltextzugriff (PDF)

The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986

Clinical genetics, 1988-06, Vol.33 (6), p.410-417

1988

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Duplication in the proximal portion of the long arm of chromosome 15, in a girl without phenotypic features of the Prader-Willi syndrome

Clinical genetics, 1984-07, Vol.26 (1), p.65-68

1984

Volltextzugriff (PDF)

A girl with 71,XXXXY karyotype

Clinical genetics, 1992-02, Vol.41 (2), p.96-99

1992

Volltextzugriff (PDF)

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER–DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCEIN SITU HYBRIDIZATION

Prenatal diagnosis, 1997-02, Vol.17 (2), p.173-179

1997

Volltextzugriff (PDF)

t(5;12)(q31;p12) A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia

Cancer genetics and cytogenetics, 1993, Vol.65 (1), p.7-11

1993

Volltextzugriff (PDF)

Effect of mast cell growth factor (c-kit ligand) on clonogenic leukemic precursor cells

Blood, 1992-08, Vol.80 (3), p.750-757

1992

Volltextzugriff (PDF)

Chimerism pattern following allogeneic bone marrow transplantation; a retrospective study of the connection with post-transplantation complications

Nederlands tijdschrift voor geneeskunde, 1990-05, Vol.134 (18), p.908

1990

Volltextzugriff (PDF)

Electronics in New Zealand

1947

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Estimation of 3-D Ocean Wave Spectra from Spotlight Sar Data During Saxon-Fpn

Classification Of Forested Terrain Using Multifrequency, Polarimetric Sap, Data

Establishment and characterization of an uveal‐melanoma cell line

Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3

Effect of subcutaneously administered human recombinant erythropoietin on erythropoiesis in patients with myelodysplasia

Effect of Mast Cell Growth Factor (c-kit ligand) on Clonogenic Leukemic Precursor Cells

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCE IN SITU HYBRIDIZATION

Amniocentesis before 14 completed weeks as an alternative to transabdominal chorionic villus sampling: a controlled trial with infant follow-up

46,XY del(18) (q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome

Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male

Chromosome abnormalities in a patient with acquired immunodeficiency syndrome (AIDS) and Burkitt lymphoma-leukemia

Monosomy 8p: an easily overlooked syndrome

A patient with an interstitial deletion of the short arm of chromosome 6

LETTER TO THE EDITOR. YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME 18 HETERMORPHISMS?

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3

Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis: A Case Report and Review of the Literature

The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986

Duplication in the proximal portion of the long arm of chromosome 15, in a girl without phenotypic features of the Prader-Willi syndrome

A girl with 71,XXXXY karyotype

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER–DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCEIN SITU HYBRIDIZATION

t(5;12)(q31;p12) A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia

Effect of mast cell growth factor (c-kit ligand) on clonogenic leukemic precursor cells

Chimerism pattern following allogeneic bone marrow transplantation; a retrospective study of the connection with post-transplantation complications

Electronics in New Zealand

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