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PITX2 controls asymmetric gonadal development in both sexes of the chick and can rescue the degeneration of the right ovary

Development (Cambridge), 2007-12, Vol.134 (23), p.4199-4208

2007

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The origin of the Mullerian duct in chick and mouse

Developmental biology, 2007-02, Vol.302 (2), p.389-398

2007

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Gonadal Asymmetry and Sex Determination in Birds

Sexual development, 2014-01, Vol.8 (5), p.227-242

2014

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Error-prone ZW pairing and no evidence for meiotic sex chromosome inactivation in the chicken germ line

PLoS genetics, 2012-03, Vol.8 (3), p.e1002560-e1002560

2012

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Oestrogen in the chick embryo can induce chromosomally male ZZ left gonad epithelial cells to form an ovarian cortex that can support oogenesis

Development (Cambridge), 2020-02, Vol.147 (4)

2020

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Primary sex determination in birds depends on DMRT1 dosage, but gonadal sex does not determine adult secondary sex characteristics

Proceedings of the National Academy of Sciences - PNAS, 2021-03, Vol.118 (10), p.1

2021

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An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

Nature (London), 1994-12, Vol.372 (6507), p.635-641

1994

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Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

Nature (London), 1994-12, Vol.372 (6507), p.672-676

1994

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RNA FISH, DNA FISH and Chromosome Painting of Chicken Oocytes

Methods in molecular biology (Clifton, N.J.), 2016-01, Vol.1457, p.191

2016

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In the chick embryo, estrogen can induce chromosomally male ZZ left gonad epithelial cells to form an ovarian cortex, which supports oogenesis

Development (Cambridge), 2020-01

2020

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Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY -related gene

Nature (London), 1994-12, Vol.372 (6506), p.525-530

1994

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The role of SOX9 in autosomal sex reversal and campomelic dysplasia

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 1995-11, Vol.350 (1333), p.271

1995

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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Nature (London), 1991-10, Vol.353 (6344), p.529-536

1991

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A New Submicroscopic Deletion That Refines the 9p Region for Sex Reversal

Genomics (San Diego, Calif.), 2000-05, Vol.65 (3), p.203-212

2000

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Mutations in SOX9, the gene responsible for campomelic dysplasia and autosomal sex reversal

American journal of human genetics, 1995-11, Vol.57 (5), p.1028-1036

1995

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Molecular Analysis of 9p Deletions Associated with XY Sex Reversal: Refining the Localization of a Sex-Determining Gene to the Tip of the Chromosome

American journal of human genetics, 1998-09, Vol.63 (3), p.905-908

1998

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22-P015 Chicken oocytes and meiotic silencing

Mechanisms of development, 2009-08, Vol.126, p.S333-S333

2009

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A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis

Genomics (San Diego, Calif.), 1991-10, Vol.11 (2), p.443-451

1991

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Campomelic Dysplasia with XY Sex Reversal: Diverse Phenotypes Resulting from Mutations in a Single Gene

Annals of the New York Academy of Sciences, 1996-06, Vol.785 (1), p.137-149

1996

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Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region

Genomics (San Diego, Calif.), 1990-10, Vol.8 (2), p.263-270

1990

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The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation

Mechanisms of development, 2000-02, Vol.90 (2), p.323-326

2000

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Campomelic Dysplasia with XY Sex Reversal: Diverse Phenotypes Resulting from Mutations in a Single Genea

Annals of the New York Academy of Sciences, 1996-06, Vol.785 (1), p.137-149

1996

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Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq

Human genetics, 1993-05, Vol.91 (4), p.333-338

1993

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A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK

Genomics (San Diego, Calif.), 1996-04, Vol.33 (2), p.185-192

1996

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Probe St35-239 (DXYS64) reveals homology between the distal ends of Xq and Yq

Genomics (San Diego, Calif.), 1991-10, Vol.11 (2), p.482-483

1991

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PITX2 controls asymmetric gonadal development in both sexes of the chick and can rescue the degeneration of the right ovary

The origin of the Mullerian duct in chick and mouse

Gonadal Asymmetry and Sex Determination in Birds

Error-prone ZW pairing and no evidence for meiotic sex chromosome inactivation in the chicken germ line

Oestrogen in the chick embryo can induce chromosomally male ZZ left gonad epithelial cells to form an ovarian cortex that can support oogenesis

Primary sex determination in birds depends on DMRT1 dosage, but gonadal sex does not determine adult secondary sex characteristics

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

RNA FISH, DNA FISH and Chromosome Painting of Chicken Oocytes

In the chick embryo, estrogen can induce chromosomally male ZZ left gonad epithelial cells to form an ovarian cortex, which supports oogenesis

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY -related gene

The role of SOX9 in autosomal sex reversal and campomelic dysplasia

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

A New Submicroscopic Deletion That Refines the 9p Region for Sex Reversal

Mutations in SOX9, the gene responsible for campomelic dysplasia and autosomal sex reversal

Molecular Analysis of 9p Deletions Associated with XY Sex Reversal: Refining the Localization of a Sex-Determining Gene to the Tip of the Chromosome

22-P015 Chicken oocytes and meiotic silencing

A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis

Campomelic Dysplasia with XY Sex Reversal: Diverse Phenotypes Resulting from Mutations in a Single Gene

Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region

The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation

Campomelic Dysplasia with XY Sex Reversal: Diverse Phenotypes Resulting from Mutations in a Single Genea

Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq

A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK

Probe St35-239 (DXYS64) reveals homology between the distal ends of Xq and Yq

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