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Molecular cytogenetic insights to the phylogenetic affinities of the giraffe (Giraffa camelopardalis) and pronghorn (Antilocapra americana)

Chromosome research, 2013-08, Vol.21 (5), p.447-460

2013

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Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

European journal of human genetics : EJHG, 2011-05, Vol.19 (5), p.540-546

2011

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A Turner syndrome neurocognitive phenotype maps to Xp22.3

Behavioral and brain functions, 2007-05, Vol.3 (1), p.24-24

2007

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Androgen Receptor CAGn Repeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome

The journal of clinical endocrinology and metabolism, 2005-09, Vol.90 (9), p.5041-5046

2005

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Cognitive and motor development during childhood in boys with Klinefelter syndrome

American journal of medical genetics. Part A, 2008-03, Vol.146A (6), p.708-719

2008

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Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

Pediatric research, 2008-10, Vol.64 (4), p.358-363

2008

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Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome

Hormone research, 2005-01, Vol.64 (1), p.39-45

2005

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The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children with Leri-Weill Dyschondrosteosis and Turner Syndrome

The Journal of pediatrics, 2005-10, Vol.147 (4), p.499-507

2005

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Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease

Journal of pediatric surgery, 2007-11, Vol.42 (11), p.1928-1932

2007

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Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

European journal of human genetics : EJHG, 2012-02, Vol.20 (2), p.249-249

2012

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Lagomorphs (rabbits, pikas and hares) do not use telomere-directed replicative aging in vitro

Mechanisms of ageing and development, 2005-06, Vol.126 (6), p.685-691

2005

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Reversal of Left-Right Asymmetry: A Situs Inversus Mutation

Science (American Association for the Advancement of Science), 1993-04, Vol.260 (5108), p.679-682

1993

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Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3

Mammalian genome, 2002-11, Vol.13 (11), p.625-632

2002

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Complete SHOX deficiency causes Langer mesomelic dysplasia

American journal of medical genetics, 2002-06, Vol.110 (2), p.158-163

2002

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Erratum: Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

European journal of human genetics : EJHG, 2012-01, Vol.20 (2), p.249-249

2012

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Androgen Receptor CAG n Repeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome

The journal of clinical endocrinology and metabolism, 2005-09, Vol.90 (9), p.5041-5046

2005

Volltextzugriff (PDF)

PRENATAL DIAGNOSIS OF UNIPARENTAL DISOMY 15 FOLLOWING TRISOMY 15 MOSAICISM

Prenatal diagnosis, 1996-04, Vol.16 (4), p.323-332

1996

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Expression of the rat liver carnitine palmitoyltransferase I (CPT-Iα) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization

Biochemical journal, 1999-06, Vol.340 (2), p.425-432

1999

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Identification of abnormal chromosomal complement in formalin-fixed, paraffin-embedded placental tissue

Prenatal diagnosis, 1995-01, Vol.15 (1), p.21-26

1995

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Rodent common fragile sites: are they conserved: evidence from mouse and rat

Chromosoma, 1989-05, Vol.97 (6), p.459-464

1989

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Fetal blood sampling demonstrating chimerism in monozygotic twins discordant for sex and tissue karyotype (46,XY and 45,X)

Prenatal diagnosis, 1990-01, Vol.10 (1), p.25-28

1990

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Neutropenia and defective chemotaxis associated with binuclear, tetraploid myeloid-monocytic leukocytes

The Journal of pediatrics, 1987-10, Vol.111 (4), p.555-558

1987

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Silver-staining patterns of mammalian epididymal spermatozoa

Cytogenetics and cell genetics, 1981, Vol.30 (3), p.157

1981

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Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17

American journal of medical genetics, 1986-04, Vol.23 (4), p.853-859

1986

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Karyotypes of Eight Species of Mexican Rodents (Muridae)

Journal of mammalogy, 1977-11, Vol.58 (4), p.479-487

1977

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Molecular cytogenetic insights to the phylogenetic affinities of the giraffe (Giraffa camelopardalis) and pronghorn (Antilocapra americana)

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

A Turner syndrome neurocognitive phenotype maps to Xp22.3

Androgen Receptor CAGn Repeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome

Cognitive and motor development during childhood in boys with Klinefelter syndrome

Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome

The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children with Leri-Weill Dyschondrosteosis and Turner Syndrome

Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

Lagomorphs (rabbits, pikas and hares) do not use telomere-directed replicative aging in vitro

Reversal of Left-Right Asymmetry: A Situs Inversus Mutation

Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3

Complete SHOX deficiency causes Langer mesomelic dysplasia

Erratum: Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

Androgen Receptor CAG n Repeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome

PRENATAL DIAGNOSIS OF UNIPARENTAL DISOMY 15 FOLLOWING TRISOMY 15 MOSAICISM

Expression of the rat liver carnitine palmitoyltransferase I (CPT-Iα) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization

Identification of abnormal chromosomal complement in formalin-fixed, paraffin-embedded placental tissue

Rodent common fragile sites: are they conserved: evidence from mouse and rat

Fetal blood sampling demonstrating chimerism in monozygotic twins discordant for sex and tissue karyotype (46,XY and 45,X)

Neutropenia and defective chemotaxis associated with binuclear, tetraploid myeloid-monocytic leukocytes

Silver-staining patterns of mammalian epididymal spermatozoa

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17

Karyotypes of Eight Species of Mexican Rodents (Muridae)

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