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Differential diagnosis between acinic cell carcinoma and pleomorphic adenoma using the quantitative parameters of contrast-enhanced ultrasound

European review for medical and pharmacological sciences, 2021-02, Vol.25 (4), p.1936

2021

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Molecular isolation and characterization of an expressed gene from the human Y chromosome

Human molecular genetics, 1992-12, Vol.1 (9), p.717-726

1992

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Unusual distribution of Zfy and Zfx sequences on the sex chromosomes of the wood lemming, a species exhibiting XY sex reversal

Cytogenetic and genome research, 1992, Vol.60 (1), p.48-54

1992

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Genomic Structure, Expression, and Chromosomal Localization of the Human Glycine N-Methyltransferase Gene

Genomics (San Diego, Calif.), 2000-05, Vol.66 (1), p.43-47

2000

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Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis

American journal of human genetics, 1992-05, Vol.50 (5), p.988-997

1992

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Mapping of genes for inhibin subunits α, βA, and βB on human and mouse chromosomes and studies of jsd mice

Genomics (San Diego, Calif.), 1989-07, Vol.5 (1), p.91-99

1989

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The pronatriodilatin gene is located on the distal short arm of human chromosome 1 and on mouse chromosome 4

American journal of human genetics, 1985-11, Vol.37 (6), p.1117-1128

1985

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Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes

Human genetics, 1992-02, Vol.88 (4), p.393-398

1992

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Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family

Clinical genetics, 1995-03, Vol.47 (3), p.125-132

1995

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A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation

Human genetics, 1995-11, Vol.96 (5), p.585-588

1995

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Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: Case report and review

American journal of medical genetics, 1995-01, Vol.55 (2), p.155-160

1995

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A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization

American journal of medical genetics, 1997-02, Vol.68 (4), p.417-420

1997

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Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy

American journal of medical genetics, 1992-11, Vol.44 (4), p.500-502

1992

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Familial dup(5)(q15q21) associated with normal and abnormal phenotypes

American journal of medical genetics, 1998-01, Vol.75 (1), p.75-77

1998

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A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1

Molecular vision, 1995-12, Vol.1, p.3-3

1995

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Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46, XY/46,XY, -18,+ dic(18)(q12.2)]

American journal of medical genetics, 1990-06, Vol.36 (2), p.247-250

1990

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Duplication of euchromatin without phenotypic effects: A variant of chromosome 16

American journal of medical genetics, 1990-05, Vol.36 (1), p.43-44

1990

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Antenatal diagnosis of 45,X/48,XYYY

American journal of medical genetics, 1989-10, Vol.34 (2), p.207-210

1989

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Regional assignments of the zinc finger Y-linked gene (ZFY) and related sequences on human and mouse chromosomes

Cytogenetic and genome research, 1990-01, Vol.54 (3-4), p.151-153

1990

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High resolution cytogenetic evaluation of couples with recurring fetal wastage

Human genetics, 1985-01, Vol.69 (3), p.246-249

1985

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Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia

American journal of medical genetics, 1997-05, Vol.70 (2), p.134-137

1997

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3; 9; 15; 22 complex translocation in an adult chronic myelocytic leukemia

Taiwan yi xue hui za zhi. Journal of the Formosan Medical Association, 1983-09, Vol.82 (9), p.1005

1983

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Phase III randomized study of second line ADI-PEG 20 plus best supportive care versus placebo plus best supportive care in patients with advanced hepatocellular carcinoma

Annals of oncology, 2018-06, Vol.29 (6), p.1402-1408

2018

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Ethnic Differences in Body Mass Index and Prevalence of Obesity in School Children of Urumqi City, Xinjiang, China

Biomedical and environmental sciences, 2006-12, Vol.19 (6), p.469-473

2006

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Nasal and sinus symptoms and chronic rhinosinusitis in a population‐based sample

Allergy (Copenhagen), 2017-02, Vol.72 (2), p.274-281

2017

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Differential diagnosis between acinic cell carcinoma and pleomorphic adenoma using the quantitative parameters of contrast-enhanced ultrasound

Molecular isolation and characterization of an expressed gene from the human Y chromosome

Unusual distribution of Zfy and Zfx sequences on the sex chromosomes of the wood lemming, a species exhibiting XY sex reversal

Genomic Structure, Expression, and Chromosomal Localization of the Human Glycine N-Methyltransferase Gene

Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis

Mapping of genes for inhibin subunits α, βA, and βB on human and mouse chromosomes and studies of jsd mice

The pronatriodilatin gene is located on the distal short arm of human chromosome 1 and on mouse chromosome 4

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes

Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family

A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation

Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: Case report and review

A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization

Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy

Familial dup(5)(q15q21) associated with normal and abnormal phenotypes

A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1

Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46, XY/46,XY, -18,+ dic(18)(q12.2)]

Duplication of euchromatin without phenotypic effects: A variant of chromosome 16

Antenatal diagnosis of 45,X/48,XYYY

Regional assignments of the zinc finger Y-linked gene (ZFY) and related sequences on human and mouse chromosomes

High resolution cytogenetic evaluation of couples with recurring fetal wastage

Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia

3; 9; 15; 22 complex translocation in an adult chronic myelocytic leukemia

Phase III randomized study of second line ADI-PEG 20 plus best supportive care versus placebo plus best supportive care in patients with advanced hepatocellular carcinoma

Ethnic Differences in Body Mass Index and Prevalence of Obesity in School Children of Urumqi City, Xinjiang, China

Nasal and sinus symptoms and chronic rhinosinusitis in a population‐based sample

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