chromosome 1p32 Latest Research Papers

Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

Molecular Cytogenetics ◽

10.1186/s13039-021-00534-5 ◽

2021 ◽

Vol 14 (1) ◽

Author(s):

Emanuele G. Coci ◽

Udo Koehler ◽

Thomas Liehr ◽

Armin Stelzner ◽

Christian Fink ◽

...

Keyword(s):

Deletion Syndrome ◽

Related Individuals ◽

Chromosome 1P32

An amendment to this paper has been published and can be accessed via the original article.

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CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Neuropediatrics ◽

10.1055/s-0036-1583695 ◽

2016 ◽

Vol 47 (S 01) ◽

Author(s):

E. Coci ◽

U. Koehler ◽

T. Liehr ◽

A. Stelzner ◽

C. Fink ◽

...

Keyword(s):

Deletion Syndrome ◽

Related Individuals ◽

Chromosome 1P32

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CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

Molecular Cytogenetics ◽

10.1186/s13039-016-0219-y ◽

2016 ◽

Vol 9 (1) ◽

Cited By ~ 4

Author(s):

Emanuele G. Coci ◽

Udo Koehler ◽

Thomas Liehr ◽

Armin Stelzner ◽

Christian Fink ◽

...

Keyword(s):

Deletion Syndrome ◽

Related Individuals ◽

Chromosome 1P32

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New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

JAMA Neurology ◽

10.1001/jamaneurol.2013.2311 ◽

2013 ◽

Vol 70 (6) ◽

pp. 764 ◽

Cited By ~ 22

Author(s):

Carmen Serrano-Munuera ◽

Marc Corral-Juan ◽

Giovanni Stevanin ◽

Hector San Nicolás ◽

Carles Roig ◽

...

Keyword(s):

Eye Movements ◽

Spinocerebellar Ataxia ◽

Chromosome 1P32

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Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/j.tjog.2011.07.014 ◽

2011 ◽

Vol 50 (3) ◽

pp. 345-352 ◽

Cited By ~ 17

Author(s):

Chih-Ping Chen ◽

Yi-Ning Su ◽

Yi-Yung Chen ◽

Schu-Rern Chern ◽

Yu-Peng Liu ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Corpus Callosum ◽

Comparative Genomic Hybridization ◽

Intrauterine Growth Restriction ◽

Array Comparative Genomic Hybridization ◽

External Genitalia ◽

Deletion Syndrome ◽

Comparative Genomic ◽

Intrauterine Growth ◽

Chromosome 1P32

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Minor Allele C of Chromosome 1p32 Single Nucleotide Polymorphism rs11206510 Confers Risk of Ischemic Stroke in the Chinese Han Population

Stroke ◽

10.1161/strokeaha.110.583096 ◽

2010 ◽

Vol 41 (8) ◽

pp. 1587-1592 ◽

Cited By ~ 24

Author(s):

Chengqi Xu ◽

Fan Wang ◽

Binbin Wang ◽

Xiuchun Li ◽

Cong Li ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Ischemic Stroke ◽

Minor Allele ◽

Chinese Han Population ◽

Nucleotide Polymorphism ◽

Chinese Han ◽

Single Nucleotide ◽

Han Population ◽

Chromosome 1P32

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Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33

The American Journal of Human Genetics ◽

10.1086/512248 ◽

2007 ◽

Vol 80 (3) ◽

pp. 539-549 ◽

Cited By ~ 26

Author(s):

Simone Sanna-Cherchi ◽

Gianluca Caridi ◽

Patricia L. Weng ◽

Monica Dagnino ◽

Marco Seri ◽

...

Keyword(s):

Renal Hypodysplasia ◽

Chromosome 1P32

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Assignment1 of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization

Cytogenetic and Genome Research ◽

10.1159/000056891 ◽

2001 ◽

Vol 92 (1-2) ◽

pp. 164-165 ◽

Cited By ~ 35

Author(s):

G. Calabrese ◽

C. Crescenzi ◽

E. Morizio ◽

G. Palka ◽

E. Guerra ◽

...

Keyword(s):

In Situ Hybridization ◽

Human Chromosome ◽

Chromosome 1P32

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Two consistently deleted regions within chromosome 1p32-pter in human non-small cell lung cancer

Molecular Carcinogenesis ◽

10.1002/mc.1023 ◽

2001 ◽

Vol 30 (3) ◽

pp. 151-158 ◽

Cited By ~ 7

Author(s):

Victor Chizhikov ◽

Irina Zborovskaya ◽

Konstantin Laktionov ◽

Vera Delektorskaya ◽

Boris Polotskii ◽

...

Keyword(s):

Lung Cancer ◽

Small Cell Lung Cancer ◽

Cell Lung Cancer ◽

Small Cell ◽

Small Cell Lung ◽

Chromosome 1P32

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Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred

Arteriosclerosis Thrombosis and Vascular Biology ◽

10.1161/01.atv.20.4.1089 ◽

2000 ◽

Vol 20 (4) ◽

pp. 1089-1093 ◽

Cited By ~ 64

Author(s):

Steven C. Hunt ◽

Paul N. Hopkins ◽

Katrina Bulka ◽

Michael T. McDermott ◽

Thomas L. Thorne ◽

...

Keyword(s):

Familial Hypercholesterolemia ◽

The Third ◽

Genetic Localization ◽

Chromosome 1P32

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chromosome 1p32
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Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction

Minor Allele C of Chromosome 1p32 Single Nucleotide Polymorphism rs11206510 Confers Risk of Ischemic Stroke in the Chinese Han Population

Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33

Assignment1 of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization

Two consistently deleted regions within chromosome 1p32-pter in human non-small cell lung cancer

Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred

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chromosome 1p32Recently Published Documents

TOTAL DOCUMENTS

H-INDEX

Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction

Minor Allele C of Chromosome 1p32 Single Nucleotide Polymorphism rs11206510 Confers Risk of Ischemic Stroke in the Chinese Han Population

Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33

Assignment1 of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization

Two consistently deleted regions within chromosome 1p32-pter in human non-small cell lung cancer

Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred

chromosome 1p32
Recently Published Documents