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Identification of the first homozygous 1‐bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing

Clinical genetics, 2018-02, Vol.93 (2), p.408-411

2018

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Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity: prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling

Human reproduction (Oxford), 2017-12, Vol.32 (12), p.2561-2573

2017

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Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion

Clinical endocrinology (Oxford), 2006-09, Vol.65 (3), p.294-300

2006

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Effects of Type 1 Insulin-Like Growth Factor Receptor Silencing in a Human Adrenocortical Cell Line

Hormone and metabolic research, 2016-07, Vol.48 (7), p.484-488

2016

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Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients

Brazilian journal of medical and biological research, 2004-01, Vol.37 (1), p.145-150

2004

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A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2870-2872

1999

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Síndrome de persistencia del conducto de Müller debido a mutación en el gen del receptor de la hormona antimülleriana (AMHR2)

Anales de pediatría (Barcelona, Spain : 2003), 2017-02, Vol.86 (2), p.94-95

2017

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Elevated plasma miR-210 expression is associated with atypical genitalia in patients with 46,XY differences in sex development

Yearbook of Paediatric Endocrinology, 2023-09

2023

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A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives

Human genetics, 1998-02, Vol.102 (2), p.213-215

1998

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Contribution of clinical and genetic approaches for diagnosing 209 index cases with 46, XY differences of sex development

Yearbook of Paediatric Endocrinology, 2022-09

2022

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Genetic disorders in prenatal onset syndromic short stature identified by exome sequencing

Yearbook of Paediatric Endocrinology, 2020-10

2020

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Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings

The journal of clinical endocrinology and metabolism, 2003-07, Vol.88 (7), p.3027-3034

2003

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ORIGINAL ARTICLE: Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion

Clinical endocrinology (Oxford), 2006-09, Vol.65 (3), p.294-300

2006

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Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue

Medical science monitor, 2001-03, Vol.7 (2), p.238-241

2001

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Comparison between parental and variant soybean Bradyrhizobium strains with regard to the production of lipo-chitin nodulation signals, early stages of root infection, nodule occupancy, and N₂ fixation rates

Plant and soil, 1996-10, Vol.186 (2), p.331-341

1996

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Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reaction

Revista do Hospital das Clinicás, 1998-03, Vol.53 (2), p.80

1998

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Comparison between parental and variant soybeanBradyrhizobium strains with regard to the production of lipo-chitin nodulation signals, early stages of root infection, nodule occupancy, and N2 fixation rates

Plant and soil, 1996-10, Vol.186 (2), p.331-341

1996

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Comparison between parental and variant soybean Bradyrhizobium strains with regard to the production of lipo-chitin nodulation signals, early stages of root infection, nodule occupancy, and N2 fixation rates

Hydrobiologia, 1996-10, Vol.186 (2), p.331-341

1996

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Morphological, physiological and genetic characterization of two new Bradyrhizobium strains recently recommended as Brazilian commercial inoculants for soybean

Symbiosis (Philadelphia, Pa.), 1996, Vol.20 (2), p.147-162

1996

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DETECTION OF THE SRY AND ZFY SLQUENCES IN PATIENTS WITH ABNORMAL GORADAL DIFFERENTIATION

Pediatric research, 1993-05, Vol.33, p.S17-S17

1993

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Detection of Y-specific sequences in 122 patients with Turner syndrome: Nested PCR is not a reliable method

American journal of medical genetics, 2002-02, Vol.107 (4), p.299-305

2002

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Stability of hydrous silicate at high pressures and water transport to the deep lower mantle

Nature geoscience, 2014-03, Vol.7 (3), p.224-227

2014

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Effect of cyclic heat loading on pure tungsten for the ITER divertor

Journal of nuclear materials, 2020-12, Vol.542, p.152509, Article 152509

2020

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Characterization of nanoscale mechanical heterogeneity in a metallic glass by dynamic force microscopy

Physical review letters, 2011-03, Vol.106 (12), p.125504-125504, Article 125504

2011

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Dietary variety and decline in lean mass and physical performance in community-dwelling older Japanese: A 4-year follow-up study

The Journal of nutrition, health & aging, 2017, Vol.21 (1), p.11-16

2017

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Identification of the first homozygous 1‐bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing

Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity: prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling

Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion

Effects of Type 1 Insulin-Like Growth Factor Receptor Silencing in a Human Adrenocortical Cell Line

Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients

A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency

Síndrome de persistencia del conducto de Müller debido a mutación en el gen del receptor de la hormona antimülleriana (AMHR2)

Elevated plasma miR-210 expression is associated with atypical genitalia in patients with 46,XY differences in sex development

A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives

Contribution of clinical and genetic approaches for diagnosing 209 index cases with 46, XY differences of sex development

Genetic disorders in prenatal onset syndromic short stature identified by exome sequencing

Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings

ORIGINAL ARTICLE: Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion

Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue

Comparison between parental and variant soybean Bradyrhizobium strains with regard to the production of lipo-chitin nodulation signals, early stages of root infection, nodule occupancy, and N₂ fixation rates

Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reaction

Comparison between parental and variant soybeanBradyrhizobium strains with regard to the production of lipo-chitin nodulation signals, early stages of root infection, nodule occupancy, and N2 fixation rates

Comparison between parental and variant soybean Bradyrhizobium strains with regard to the production of lipo-chitin nodulation signals, early stages of root infection, nodule occupancy, and N2 fixation rates

Morphological, physiological and genetic characterization of two new Bradyrhizobium strains recently recommended as Brazilian commercial inoculants for soybean

DETECTION OF THE SRY AND ZFY SLQUENCES IN PATIENTS WITH ABNORMAL GORADAL DIFFERENTIATION

Detection of Y-specific sequences in 122 patients with Turner syndrome: Nested PCR is not a reliable method

Stability of hydrous silicate at high pressures and water transport to the deep lower mantle

Effect of cyclic heat loading on pure tungsten for the ITER divertor

Characterization of nanoscale mechanical heterogeneity in a metallic glass by dynamic force microscopy

Dietary variety and decline in lean mass and physical performance in community-dwelling older Japanese: A 4-year follow-up study

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