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Small mammals (Rodentia) present in Tyto furcata (Temminck, 1827) (Strigiformes, Tytonidae) pellets from the Reserva Natural da Guaricica, Antonina, coastal Paraná, Brazil

Brazilian journal of biology, 2023, Vol.83, p.1-3

2023

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A review of bush dog Speothos venaticus (Lund, 1842) (Carnivora, Canidae) occurrences in Paraná state, subtropical Brazil

Brazilian journal of biology, 2016-06, Vol.76 (2), p.444-449

2016

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Small mammals (Rodentia) present in Tyto furcata (Temminck, 1827) (Strigiformes, Tytonidae) pellets from the Reserva Natural da Guaricica, Antonina, coastal Paraná, Brazil

Brazilian journal of biology, 2023, Vol.83

2023

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Genetic heterogeneity for a Nijmegen breakage-like syndrome

Clinical genetics, 2003-04, Vol.63 (4), p.283-290

2003

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A review of bush dog Speothos venaticus (Lund, 1842) (Carnivora, Canidae) occurrences in Paraná state, subtropical Brazil/Revisão dos registros de ocorrência do cachorro-do-mato-vinagre Speothos venaticus (Lund, 1842) (Carnivora, Canidae), no Estado do Paraná, Brasil Subtropical

Brazilian journal of biology, 2016-04, Vol.76 (2), p.444-444

2016

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A novel mutation and novel features in Nijmegen breakage syndrome

Journal of medical genetics, 2001-02, Vol.38 (2), p.113-117

2001

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Ring chromosome 9 with a 9p22.3-p24.3 duplication

European journal of pediatrics, 1999-10, Vol.158 (10), p.791-793

1999

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A computational model of tense selection and its experimentation within an intelligent tutor

Trends in Artificial Intelligence, 2005, p.261-270

2005

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Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome

Journal of medical genetics, 1988-03, Vol.25 (3), p.173-180

1988

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Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm

Human genetics, 1976-01, Vol.34 (2), p.119-124

1976

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Abnormal methylation does not prevent X inactivation in ICF patients

Cytogenetics and cell genetics, 1999, Vol.84 (3-4), p.245

1999

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A complex chromosome rearrangement with 10 breakpoints: tentative assignment of the locus for Williams syndrome to 4q33----q35.1

Journal of medical genetics, 1992-04, Vol.29 (4), p.253-255

1992

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XX sex reversal, palmoplantar keratoderma, and predisposition to squamous cell carcinoma: Genetic analysis in one family

American journal of medical genetics. Part A, 2005-10, Vol.138A (3), p.241-246

2005

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Molecular analysis of a human Y;1 translocation in an azoospermic male

Cytogenetics and cell genetics, 1994, Vol.65 (4), p.256

1994

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Chromosome instability and nibrin protein variants in NBS heterozygotes

European journal of human genetics : EJHG, 2003-04, Vol.11 (4), p.297-303

2003

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Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy

Journal of medical genetics, 1996-05, Vol.33 (5), p.366-370

1996

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Population survey of the marsh deer Blastocerus dichotomus (Mammalia, Cervidae) in the Ilha Grande National Park and surroundings: conservation implications

Iheringia. Série zoologia, 2010-06, Vol.100 (2), p.111-115

2010

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Interphase cytogenetics of the ICF syndrome

Annals of human genetics, 1992-07, Vol.56 (3), p.273-278

1992

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The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype: Report of 11 patients and delineation of the clinical picture

Human genetics, 1981-04, Vol.57 (2)

1981

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Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts

Journal of medical genetics, 1989-07, Vol.26 (7), p.452-456

1989

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Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation

Human genetics, 1982, Vol.61 (4), p.364-368

1982

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Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

Human genetics, 1980-01, Vol.54 (2), p.205-206

1980

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Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression

Journal of medical genetics, 1998-09, Vol.35 (9), p.778-783

1998

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Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency

Human genetics, 1979-10, Vol.51 (2), p.127-137

1979

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Corpus callosum hypoplasia and associated brain anomalies in Nijmegen breakage syndrome

Journal of medical genetics, 2002-05, Vol.39 (5), p.e25-25

2002

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Small mammals (Rodentia) present in Tyto furcata (Temminck, 1827) (Strigiformes, Tytonidae) pellets from the Reserva Natural da Guaricica, Antonina, coastal Paraná, Brazil

A review of bush dog Speothos venaticus (Lund, 1842) (Carnivora, Canidae) occurrences in Paraná state, subtropical Brazil

Small mammals (Rodentia) present in Tyto furcata (Temminck, 1827) (Strigiformes, Tytonidae) pellets from the Reserva Natural da Guaricica, Antonina, coastal Paraná, Brazil

Genetic heterogeneity for a Nijmegen breakage-like syndrome

A review of bush dog Speothos venaticus (Lund, 1842) (Carnivora, Canidae) occurrences in Paraná state, subtropical Brazil/Revisão dos registros de ocorrência do cachorro-do-mato-vinagre Speothos venaticus (Lund, 1842) (Carnivora, Canidae), no Estado do Paraná, Brasil Subtropical

A novel mutation and novel features in Nijmegen breakage syndrome

Ring chromosome 9 with a 9p22.3-p24.3 duplication

A computational model of tense selection and its experimentation within an intelligent tutor

Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome

Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm

Abnormal methylation does not prevent X inactivation in ICF patients

A complex chromosome rearrangement with 10 breakpoints: tentative assignment of the locus for Williams syndrome to 4q33----q35.1

XX sex reversal, palmoplantar keratoderma, and predisposition to squamous cell carcinoma: Genetic analysis in one family

Molecular analysis of a human Y;1 translocation in an azoospermic male

Chromosome instability and nibrin protein variants in NBS heterozygotes

Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy

Population survey of the marsh deer Blastocerus dichotomus (Mammalia, Cervidae) in the Ilha Grande National Park and surroundings: conservation implications

Interphase cytogenetics of the ICF syndrome

The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype: Report of 11 patients and delineation of the clinical picture

Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts

Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation

Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression

Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency

Corpus callosum hypoplasia and associated brain anomalies in Nijmegen breakage syndrome

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