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Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis

Haematologica (Roma), 2011-08, Vol.96 (8), p.1144-1152

2011

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High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy

Clinical genetics, 2016-01, Vol.89 (1), p.82-87

2016

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Application of chromosomal microarray in the evaluation of abnormal prenatal findings

Clinical genetics, 2013-07, Vol.84 (1), p.47-54

2013

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Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations

Placenta (Eastbourne), 2011-05, Vol.32 (5), p.409-412

2011

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Complex chromosome lesion delineated by array CGH in a woman with primary ovarian insufficiency

Fertility and sterility, 2010, Vol.94 (4), p.S41-S41

2010

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Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

Journal of medical genetics, 2006-08, Vol.43 (8), p.660-664

2006

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Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

American journal of human genetics, 1996-02, Vol.58 (2), p.335-346

1996

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Comparative study of primary and recurrent ovarian serous carcinomas: comparative genomic hybridization analysis with a potential application for prognosis

Gynecologic oncology, 2003-06, Vol.89 (3), p.369-375

2003

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Follicular lymphoma-like B cells of uncertain significance (in situ follicular lymphoma) may infrequently progress, but precedes follicular lymphoma, is associated with other overt lymphomas and mimics follicular lymphoma in flow cytometric studies

Haematologica (Roma), 2013-10, Vol.98 (10), p.1571-1580

2013

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P–553 Women with molar pregnancies have a genetic susceptibility to aneuploid miscarriages

Human reproduction (Oxford), 2021-08, Vol.36 (Supplement_1)

2021

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Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients

American journal of human genetics, 1995-07, Vol.57 (1), p.40-48

1995

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Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus

The EMBO journal, 1988-03, Vol.7 (3), p.727-738

1988

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Large-scale genotyping of complex DNA

Nature biotechnology, 2003-10, Vol.21 (10), p.1233-1237

2003

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NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

Journal of medical genetics, 2011-08, Vol.48 (8), p.540-548

2011

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Cryptic duplication of 12q24.33 → qter in a child with Angelman syndrome—simultaneous occurrence of two unrelated cytogenetic events

American journal of medical genetics. Part A, 2007-05, Vol.143A (9), p.985-994

2007

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Parental Origin and Phenotype of Triploidy in Spontaneous Abortions: Predominance of Diandry and Association with the Partial Hydatidiform Mole

American journal of human genetics, 2000-06, Vol.66 (6), p.1807-1820

2000

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Genotype-phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations

Genetics in medicine, 2009-11, Vol.11 (11), p.797-805

2009

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Small marker X chromosomes lack the X inactivation center : implications for karyotype/phenotype correlations

American journal of human genetics, 1994-07, Vol.55 (1), p.87-95

1994

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Defining the borders of splenic marginal zone lymphoma: a multiparameter study

Human pathology, 2010-04, Vol.41 (4), p.540-551

2010

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Uterine Leiomyomas: Cytogenetic and Histologic Profile

Obstetrics and gynecology (New York. 1953), 1992-08, Vol.80 (2), p.209-217

1992

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The clinical use of karyotyping spontaneous abortions

American journal of obstetrics and gynecology, 2003-08, Vol.189 (2), p.397-400

2003

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The physical organization of the human immunoglobulin heavy chain gene complex

The EMBO journal, 1990-10, Vol.9 (10), p.3303-3313

1990

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Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype

Prenatal diagnosis, 2005-11, Vol.25 (11), p.1048-1056

2005

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Clinicopathologic, immunophenotypic, and molecular cytogenetic fluorescence in situ hybridization analysis of primary and secondary cutaneous follicular lymphomas

The American journal of surgical pathology, 2005, Vol.29 (1), p.69-82

2005

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Cytogenetic Abnormalities Detected by Fluorescence In Situ Hybridization on Paraffin-Embedded Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Lymphoid Tissue Biopsy Specimens

American journal of clinical pathology, 2008-10, Vol.130 (4), p.620-627

2008

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Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis

High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy

Application of chromosomal microarray in the evaluation of abnormal prenatal findings

Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations

Complex chromosome lesion delineated by array CGH in a woman with primary ovarian insufficiency

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

Comparative study of primary and recurrent ovarian serous carcinomas: comparative genomic hybridization analysis with a potential application for prognosis

Follicular lymphoma-like B cells of uncertain significance (in situ follicular lymphoma) may infrequently progress, but precedes follicular lymphoma, is associated with other overt lymphomas and mimics follicular lymphoma in flow cytometric studies

P–553 Women with molar pregnancies have a genetic susceptibility to aneuploid miscarriages

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients

Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus

Large-scale genotyping of complex DNA

NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

Cryptic duplication of 12q24.33 → qter in a child with Angelman syndrome—simultaneous occurrence of two unrelated cytogenetic events

Parental Origin and Phenotype of Triploidy in Spontaneous Abortions: Predominance of Diandry and Association with the Partial Hydatidiform Mole

Genotype-phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations

Small marker X chromosomes lack the X inactivation center : implications for karyotype/phenotype correlations

Defining the borders of splenic marginal zone lymphoma: a multiparameter study

Uterine Leiomyomas: Cytogenetic and Histologic Profile

The clinical use of karyotyping spontaneous abortions

The physical organization of the human immunoglobulin heavy chain gene complex

Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype

Clinicopathologic, immunophenotypic, and molecular cytogenetic fluorescence in situ hybridization analysis of primary and secondary cutaneous follicular lymphomas

Cytogenetic Abnormalities Detected by Fluorescence In Situ Hybridization on Paraffin-Embedded Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Lymphoid Tissue Biopsy Specimens

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