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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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Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

Oncogene, 1999-01, Vol.18 (2), p.543-550

1999

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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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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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Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

Cytogenetic and genome research, 1990-01, Vol.53 (2-3), p.126-128

1990

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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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Monosomy 8p: an easily overlooked syndrome

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

1986

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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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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

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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

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A girl with 71,XXXXY karyotype

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

1992

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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

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A second case of hexasomy 8 in myelodysplastic syndrome

Cancer genetics and cytogenetics, 1997-11, Vol.99 (1), p.68-72

1997

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A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia

Cancer genetics and cytogenetics, 1996-07, Vol.89 (2), p.132-135

1996

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Brief clinical report: a patient with dup(10p) del (8q) and Pendred syndrome

American journal of medical genetics, 1986-06, Vol.24 (2), p.211-217

1986

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

Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

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

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

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

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

Monosomy 8p: an easily overlooked syndrome

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

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

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

A second case of hexasomy 8 in myelodysplastic syndrome

A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia

Brief clinical report: a patient with dup(10p) del (8q) and Pendred syndrome

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