Disorders of sex development in Wolf-Hirschhorn syndrome: a genotype-phenotype correlation and MSX1 as candidate gene.

Rjiba, Khouloud; Ayech, Hédia; Kraiem, Olfa; Slimani, Wafa; Jelloul, Afef; Ben Hadj Hmida, Imen; Mahdhaoui, Nabiha; Saad, Ali; Mougou-Zerelli, Soumaya

Rjiba, Khouloud; Ayech, Hédia; Kraiem, Olfa; Slimani, Wafa; Jelloul, Afef; Ben Hadj Hmida, Imen; Mahdhaoui, Nabiha; Saad, Ali; Mougou-Zerelli, Soumaya.

Afiliação

Rjiba K; Laboratory of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Teaching Hospital, Sousse, Tunisia.
Ayech H; Higher Institute of Biotechnology, Monastir University, Monastir, Tunisia.
Kraiem O; Unité de Services Communs en Génétique Humaine, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Slimani W; Pediatric Department, Farhat Hached University Teaching Hospital, Sousse, Tunisia.
Jelloul A; Pediatric Department, Regional Hospital, Kairouan, Tunisia.
Ben Hadj Hmida I; Laboratory of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Teaching Hospital, Sousse, Tunisia.
Mahdhaoui N; Higher Institute of Biotechnology, Monastir University, Monastir, Tunisia.
Saad A; Unité de Services Communs en Génétique Humaine, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Mougou-Zerelli S; Laboratory of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Teaching Hospital, Sousse, Tunisia.

Mol Cytogenet ; 14(1): 12, 2021 Feb 24.

Article em En | MEDLINE | ID: mdl-33627176

Palavras-chave

Array CGH; FISH; Hypospadias; MSX1gene; WolfHirschhorn syndrome

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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Mol Cytogenet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Tunísia