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Mutations in SIP1 , encoding Smad interacting protein-1, cause a form of Hirschsprung disease

Nature genetics, 2001-04, Vol.27 (4), p.369-370

2001

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Exposure to bisphenol A is associated with recurrent miscarriage

Human reproduction (Oxford), 2005-08, Vol.20 (8), p.2325-2329

2005

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Ectopic Expression of MAFB Gene in Human Myeloma Cells Carrying (14;20)(q32;q11) Chromosomal Translocations

Cancer science, 2001-06, Vol.92 (6), p.638-644

2001

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PCBs, Hexachlorobenzene and DDE are not Associated with Recurrent Miscarriage

American journal of reproductive immunology (1989), 2003-12, Vol.50 (6), p.485-489

2003

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Twin pregnancy with chromosomal abnormalities mimicking a gestational trophoblastic disorder and coexistent foetus on ultrasound

Journal of obstetrics and gynaecology, 2018-10, Vol.38 (7), p.1023-1025

2018

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Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion

Journal of human genetics, 2005-03, Vol.50 (3), p.112-117

2005

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Genomic Organization and Expression Pattern of Mouse Neuroglycan C in the Cerebellar Development

The Journal of biological chemistry, 2000-01, Vol.275 (1), p.337-342

2000

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Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion

Journal of human genetics, 2004-04, Vol.49 (4), p.177-181

2004

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Parental origin and cell stage of non-disjunction of double trisomy in spontaneous abortion

Congenital anomalies, 2005-03, Vol.45 (1), p.21-25

2005

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Test BR625

Formal methods in system design, 2012-11

2012

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Nonsense and Frameshift Mutations in ZFHX1B, Encoding Smad-Interacting Protein 1, Cause a Complex Developmental Disorder with a Great Variety of Clinical Features

American journal of human genetics, 2001-12, Vol.69 (6), p.1178-1185

2001

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Inhibition of Nuclear Factor-κB-mediated Transcription by Association with the Amino-terminal Enhancer of Split, a Groucho-related Protein Lacking WD40 Repeats

The Journal of biological chemistry, 2000-02, Vol.275 (6), p.4383-4390

2000

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Disruption of the Hypoxanthine-Guanine Phosphoribosyl-Transferase Gene Caused by a Translocation in a Patient with Lesch-Nyhan Syndrome

Nucleosides, nucleotides & nucleic acids, 2004-10, Vol.23 (8-9), p.1173-1176

2004

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Cloning and chromosomal mapping of the human gene of neuroglycan C (NGC), a neural transmembrane chondroitin sulfate proteoglycan with an EGF module

Neuroscience research, 1998-12, Vol.32 (4), p.313-322

1998

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Searching for Genes for Cleft Lip and/or Palate Based on Breakpoint Analysis of a Balanced Translocation t(9;17)(q32;q12)

The Cleft palate-craniofacial journal, 2009-09, Vol.46 (5), p.532-540

2009

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Robertsonian metacentrics of the house musk shrew (Suncus murinus, Insectivora, Soricidae) lose the telomeric sequences in the centromeric area

Genes & Genetic Systems, 2000, Vol.75(3), pp.155-158

2000

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Genomic organization and chromosomal distribution of rat ID elements

Genes & Genetic Systems, 2001, Vol.76(4), pp.213-220

2001

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Mechanism of malsegregations at meiosis: premature centromere separation and precocious division in female Chinese hamsters stimulated with gonadotropic hormones

Congenital anomalies, 2000-09, Vol.40 (3), p.162-168

2000

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cDNA Cloning and Chromosomal Mapping of Rat Smad2 and Smad4 and Their Expression in Cultured Rat Articular Chondrocytes

Endocrine Journal, 1999, Vol.46(5), pp.695-701

1999

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Protocadherin 2C: A New Member of the Protocadherin 2 Subfamily Expressed in a Redundant Manner with OL-Protocadherin in the Developing Brain

Biochemical and biophysical research communications, 1999-07, Vol.260 (3), p.641-645

1999

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Origin of the adjacent 1 disjunction

Journal of human genetics, 1993-09, Vol.38 (3), p.345-349

Sonta, S

1993

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Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlation

Human mutation, 2001-09, Vol.18 (3), p.253-253

2001

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Developmental arrest at early stages of Chinese hamster embryos homozygous for chromosomal rearrangements

Developmental biology, 1991-03, Vol.144 (1), p.30-37

1991

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The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32

Journal of human genetics, 1998-02, Vol.43 (1), p.32-36

1998

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Comparative Analysis of the Karyotypes of the Greater Long-Tailed Hamster and the Chinese Hamster

CYTOLOGIA, 1997/09/25, Vol.62(3), pp.315-321

1997

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Mutations in SIP1 , encoding Smad interacting protein-1, cause a form of Hirschsprung disease

Exposure to bisphenol A is associated with recurrent miscarriage

Ectopic Expression of MAFB Gene in Human Myeloma Cells Carrying (14;20)(q32;q11) Chromosomal Translocations

PCBs, Hexachlorobenzene and DDE are not Associated with Recurrent Miscarriage

Twin pregnancy with chromosomal abnormalities mimicking a gestational trophoblastic disorder and coexistent foetus on ultrasound

Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion

Genomic Organization and Expression Pattern of Mouse Neuroglycan C in the Cerebellar Development

Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion

Parental origin and cell stage of non-disjunction of double trisomy in spontaneous abortion

Test BR625

Nonsense and Frameshift Mutations in ZFHX1B, Encoding Smad-Interacting Protein 1, Cause a Complex Developmental Disorder with a Great Variety of Clinical Features

Inhibition of Nuclear Factor-κB-mediated Transcription by Association with the Amino-terminal Enhancer of Split, a Groucho-related Protein Lacking WD40 Repeats

Disruption of the Hypoxanthine-Guanine Phosphoribosyl-Transferase Gene Caused by a Translocation in a Patient with Lesch-Nyhan Syndrome

Cloning and chromosomal mapping of the human gene of neuroglycan C (NGC), a neural transmembrane chondroitin sulfate proteoglycan with an EGF module

Searching for Genes for Cleft Lip and/or Palate Based on Breakpoint Analysis of a Balanced Translocation t(9;17)(q32;q12)

Robertsonian metacentrics of the house musk shrew (Suncus murinus, Insectivora, Soricidae) lose the telomeric sequences in the centromeric area

Genomic organization and chromosomal distribution of rat ID elements

Mechanism of malsegregations at meiosis: premature centromere separation and precocious division in female Chinese hamsters stimulated with gonadotropic hormones

cDNA Cloning and Chromosomal Mapping of Rat Smad2 and Smad4 and Their Expression in Cultured Rat Articular Chondrocytes

Protocadherin 2C: A New Member of the Protocadherin 2 Subfamily Expressed in a Redundant Manner with OL-Protocadherin in the Developing Brain

Origin of the adjacent 1 disjunction

Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlation

Developmental arrest at early stages of Chinese hamster embryos homozygous for chromosomal rearrangements

The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32

Comparative Analysis of the Karyotypes of the Greater Long-Tailed Hamster and the Chinese Hamster

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