Works matching IS 16615425 AND DT 2022 AND VI 16 AND IP 1

Results: 12

Erratum.
Published in:
2022
Publication type:
Correction Notice
9th International Symposium in Disorders/Differences of Sex Development.
Published in:
Sexual Development, 2022, v. 16, n. 1, p. 1, doi. 10.1159/000525564
Publication type:
Article
Front & Back Matter.
Published in:
Sexual Development, 2022, v. 16, n. 1, p. 1, doi. 10.1159/000521955
Publication type:
Article
Erratum.
Published in:
2022
Publication type:
Correction Notice
3β-Hydroxysteroid Dehydrogenase Type 2 (3βHSD2) Deficiency due to a Novel Compound Heterozygosity of a Missense Mutation (p.Thr259Met) and Frameshift Deletion (p.Lys273ArgFs*7) in an Undervirilized Infant Male with Salt Wasting.
Published in:
Sexual Development, 2022, v. 16, n. 1, p. 64, doi. 10.1159/000519062
By:
- Leka-Emiri, Sofia;
- Taibi, Ludmia;
- Mavroeidi, Vasiliki;
- Vlachopapadopoulou, Elpis A.;
- Kafetzi, Maria;
- Michalacos, Stefanos;
- de Roux, Nicolas
Publication type:
Article
Clinical, Biochemical, and Molecular Characterization of Indian Children with Clinically Suspected Androgen Insensitivity Syndrome.
Published in:
Sexual Development, 2022, v. 16, n. 1, p. 34, doi. 10.1159/000519047
By:
- Kumar, Anil;
- Sharma, Rajni;
- Faruq, Mohammed;
- Kumar, Manoj;
- Sharma, Shilpa;
- Werner, Ralf;
- Hiort, Olaf;
- Vandana, Jain
Publication type:
Article
Genetic and Epigenetic Control of Puberty.
Published in:
Sexual Development, 2022, v. 16, n. 1, p. 1, doi. 10.1159/000519039
By:
- Manotas, María Carolina;
- González, Daniel Mauricio;
- Céspedes, Camila;
- Forero, Catalina;
- Rojas Moreno, Adriana Patricia
Publication type:
Article
Can Boys Have Turner Syndrome? More than a Question of Semantics.
Published in:
Sexual Development, 2022, v. 16, n. 1, p. 19, doi. 10.1159/000518092
By:
- Knoll, Michelle M.;
- Strickland, Julie;
- Jacobson, Jill D.
Publication type:
Article
WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease.
Published in:
2022
By:
- Ferrari, Maria T.M.;
- Watanabe, Andreia;
- da Silva, Thatiane E.;
- Gomes, Nathalia L.;
- Batista, Rafael L.;
- Nishi, Mirian Y.;
- de Paula, Leila C.P.;
- Costa, Eduardo C.;
- Costa, Elaine M.F.;
- Cukier, Priscilla;
- Onuchic, Luiz F.;
- Mendonca, Berenice B.;
- Domenice, Sorahia
Publication type:
Case Study
A Nationwide Study of the Prevalence and Initial Management of Atypical Genitalia in the Newborn in Scotland.
Published in:
2022
By:
- Rodie, Martina E.;
- Ali, Salma R.;
- Jayasena, Arundathi;
- Alenazi, Naser R.;
- McMillan, Martin;
- Cox, Kathryn;
- Cassim, Sumaiya M.;
- Henderson, Stuart;
- McGowan, Ruth;
- Ahmed, S. Faisal
Publication type:
Case Study
A Small Supernumerary Xp Marker Chromosome Including Genes NR0B1 and MAGEB Causing Partial Gonadal Dysgenesis and Gonadoblastoma.
Published in:
2022
By:
- Nishi, Mirian Yumie;
- Faria Júnior, José Antônia Diniz;
- Krepischi, Ana Cristina Victorino;
- de Moraes, Daniela Rodrigues;
- da Costa, Silvia Souza;
- Silva, Elinaelma Suelane do Nascimento;
- Costa, Elaine Maria Frade;
- Mendonca, Berenice Bilharinho;
- Domenice, Sorahia
Publication type:
Case Study
Variants in 46,XY DSD-Related Genes in Syndromic and Non-Syndromic Small for Gestational Age Children with Hypospadias.
Published in:
Sexual Development, 2022, v. 16, n. 1, p. 27, doi. 10.1159/000518091
By:
- Leitao Braga, Barbara;
- Lisboa Gomes, Nathalia;
- Nishi, Mirian Y.;
- Freire, Bruna L.;
- Batista, Rafael L.;
- D. Faria Junior, Jose A.;
- Funari, Mariana F.A.;
- Figueredo Benedetti, Anna F.;
- de Moraes Narcizo, Amanda;
- Cavalca Cardoso, Lais;
- Lerario, Antonio M.;
- Guerra-Junior, Gil;
- Frade Costa, Elaine M.;
- Domenice, Sorahia;
- Jorge, Alexander A.L.;
- Mendonca, Berenice B.
Publication type:
Article