Works matching IS 16615425 AND DT 2023 AND VI 17 AND IP 1

Results: 9

Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls.

Published in:

Sexual Development, 2023, v. 17, n. 1, p. 16, doi. 10.1159/000526997

By:

Guaragna-Filho, Guilherme;
Guerra-Junior, Gil;
Tadokoro-Cuccaro, Rieko;
Hughes, Ieuan A.;
Barros, Beatriz A.;
Hiort, Olaf;
Balsamo, Antonio;
Guran, Tulay;
Holterhus, Paul M.;
Hannema, Sabine;
Poyrazoglu, Sukran;
Darendeliler, Feyza;
Bryce, Jillian;
Ahmed, S. Faisal;
Quigley, Charmian A.

Publication type:

Article

Whole-Exome Sequencing Indicated New Candidate Genes Associated with Unilateral Cryptorchidism in Pigs.

Published in:

Sexual Development, 2023, v. 17, n. 1, p. 56, doi. 10.1159/000528360

By:

da Silva, Arthur Nery;
Ibelli, Adriana Mércia Guaratini;
Savoldi, Igor Ricardo;
Cantão, Maurício Egídio;
Zanella, Eraldo Lourenso;
Marques, Mariana Groke;
da Silva, Marcos Vinicius Gualberto Barbosa;
de Peixoto, Jane Oliveira;
Ledur, Mônica Corrêa;
Lopes, Jader Silva;
Vargas, José Eduardo;
Zanella, Ricardo

Publication type:

Article

Genetic Variants in SRD5A2 in a Spectrum of DSD Patients from Australian Clinics Highlight Importance of Genetic Testing alongside Typical First-Line Investigations.

Published in:

Sexual Development, 2023, v. 17, n. 1, p. 8, doi. 10.1159/000527754

By:

Robevska, Gorjana;
Hanna, Chloe;
van den Bergen, Jocelyn;
Welch, John;
Couper, Jennifer;
Harris, Shannon;
Joshi, Kriti;
Brown, Justin;
Sabin, Matthew;
Sinclair, Andrew;
O'Connell, Michele;
Ayers, Katie

Publication type:

Article

A Surgical and Clinical Approach to Persistent Müllerian Duct Syndrome: Laparoscopic, Histological, and Molecular Findings.

Published in:

2023

By:

Mattone, María Celeste;
Lobo de la Vega, María Victoria;
Redondo, Emiro J.;
D'Alessandro, Pablo;
Perez Garrido, Natalia;
Galluzzo, María Laura;
Costanzo, Mariana;
Zaidman, Verónica;
Lazzati, Juan Manuel;
Berensztein, Esperanza;
Ramirez, Pablo;
Marino, Roxana;
Belgorosky, Alicia;
Ciaccio, Marta;
Bailez, Marcela;
Guercio, Gabriela

Publication type:

Case Study

Front & Back Matter.

Published in:: Sexual Development, 2023, v. 17, n. 1, p. 1, doi. 10.1159/000533451
Publication type:: Article

Phenotypic Variation in 46,XX Disorders of Sex Development due to the Fourth Zinc Finger Domain Variant of WT1: A Familial Case Report.

Published in:

2023

By:

Kirino, Shizuka;
Yogi, Analia;
Adachi, Eriko;
Nakatani, Hisae;
Gau, Maki;
Iemura, Ryosei;
Yamano, Haruki;
Kanamori, Toru;
Mori, Takayasu;
Sohara, Eisei;
Uchida, Shinichi;
Okamoto, Kentaro;
Udagawa, Tomohiro;
Takasawa, Kei;
Morio, Tomohiro;
Kashimada, Kenichi

Publication type:

Case Study

Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1–6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.

Published in:

2023

By:

Dundar, Ismail;
Akinci, Aysehan;
Camtosun, Emine;
Ciftci, Nurdan;
Kayas, Leman

Publication type:

Case Study

Testicular Architecture of Men with 46,XX Testicular Disorders of Sex Development.

Published in:

Sexual Development, 2023, v. 17, n. 1, p. 32, doi. 10.1159/000528955

By:

Hiort, Mirkka;
Rohayem, Julia;
Knaf, Regine;
Laurentino, Sandra;
Berglund, Agnethe;
Gravholt, Claus H.;
Gromoll, Jörg;
Wistuba, Joachim

Publication type:

Article

Targeted Next-Generation Sequencing for the Diagnosis of Gene Variants in Patients with 46,XY Disorder of Sex Development.

Published in:

Sexual Development, 2023, v. 17, n. 1, p. 26, doi. 10.1159/000528916

By:

Guo, Qiang;
Zhong, Wen Wen;
Lai, Hua Jian;
Ye, Lei;
Zhang, Yi Fei;
Li, Jun Tao;
Qiu, Jian Guang;
Wang, De Juan

Publication type:

Article