[图书][B] Zwitter beim Namen nennen: Intersexualität zwischen Pathologie, Selbstbestimmung und leiblicher Erfahrung
K Zehnder - 2010 - degruyter.com
EINFÜHRUNG 13 auf meine Annoncen jemand melden würde, und Kontakt-oder
Selbsthilfegruppen seien ihnen keine bekannt. Über die Ärzte waren also keine Kontakte …
Selbsthilfegruppen seien ihnen keine bekannt. Über die Ärzte waren also keine Kontakte …
Contribution of cytogenetic and molecular biology in disorders of sex development diagnosis: About 55 cases
FD Gueye, DIA Fatimatou, A Ndiaye… - … Journal of Genetics …, 2023 - academicjournals.org
Disorders of sex development (DSD) when diagnosed early is important as it pose a real
public health problem in Senegal. Among the supporting tools, molecular ones, which are …
public health problem in Senegal. Among the supporting tools, molecular ones, which are …
Homem XX: relato de três casos na faixa etária pediátrica
D Damiani, DR Guedes, D Damiani… - … de Endocrinologia & …, 2005 - SciELO Brasil
São apresentados três pacientes com a condição clínica conhecida como" homem XX", rara
na faixa etária pediátrica, caracterizada por um fenótipo masculino (em geral não associado …
na faixa etária pediátrica, caracterizada por um fenótipo masculino (em geral não associado …
46, XX male: clinical, hormonal/genetic findings
G Castineyra, S Copelli, O Levalle - Archives of andrology, 2002 - Taylor & Francis
The clinical genetics and hormonal status of the 46, XX male is well determined. This is a
rare condition that affects one out 20,000 male births. This study evaluates 5 infertile patients …
rare condition that affects one out 20,000 male births. This study evaluates 5 infertile patients …
XX male: 3 case reports during childhood
D Damiani, DR Guedes, D Damiani… - … de Endocrinologia & …, 2005 - SciELO Brasil
São apresentados três pacientes com a condição clínica conhecida como" homem XX", rara
na faixa etária pediátrica, caracterizada por um fenótipo masculino (em geral não associado …
na faixa etária pediátrica, caracterizada por um fenótipo masculino (em geral não associado …
[图书][B] Development of the adreno-genital system : female sex determination, ovarian and adrenal gland ontogeny regulated by Wnt-4 in mice
M Heikkilä - 2002 - oulurepo.oulu.fi
Although the genetic sex of an embryo is determined at conception by the presence or
absence of the Y chromosome, both females and males have bipotential, undifferentiated …
absence of the Y chromosome, both females and males have bipotential, undifferentiated …
Disorders of sex determination and differentiation
CA Quigley - Principles of molecular medicine, 1998 - Springer
Sex determination and differentiation are distinct, consecutive processes that follow the
establishment of chromosomal sex at the time of fertilization. The term “sex determination” …
establishment of chromosomal sex at the time of fertilization. The term “sex determination” …
Desarrollo genital prenatal. Clasificación, diagnóstico y manejo de las anomalías de la diferenciación sexual
MP Mateo, FP Rodríguez, AR Villatoro… - Clínica e Investigación …, 2023 - Elsevier
Revisión de la etiopatogenia y clasificación de las anomalías de la diferenciación sexual,
así como del desarrollo genital prenatal, para que resulte de utilidad en la evaluación y …
así como del desarrollo genital prenatal, para que resulte de utilidad en la evaluación y …
SRY-positive 46, XX male with cryptorchidism as the only presenting clinical feature
M Moreno-García, J Sánchez del Pozo… - Urologia …, 2003 - karger.com
The SRY gene, located on the short arm of the Y chromosome, is responsible for
differentiation of the testis from the undifferentiated gonad. We report a 4-year-old patient …
differentiation of the testis from the undifferentiated gonad. We report a 4-year-old patient …
Síndrome de Frasier:¿ Cómo diagnosticar una enfermedad rara en la consulta de Ginecología? Reporte de caso
M Muñoz-Infante, M Pineda-Mateo… - … y obstetricia de …, 2023 - scielo.org.mx
Resumen INTRODUCCIÓN: El síndrome de Frasier es una enfermedad de herencia
autosómica dominante con una prevalencia inferior a 1 caso por cada millón de recién …
autosómica dominante con una prevalencia inferior a 1 caso por cada millón de recién …