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

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作者： Khouloud,Rjiba ^[1] ; Hédia,Ayech ^[2] ; Olfa,Kraiem ^[3] ; Wafa,Slimani ^[4] ; Afef,Jelloul ^[5] ; Imen,Ben Hadj Hmida ^[1] ; Nabiha,Mahdhaoui ^[2] ; Ali,Saad ^[3] ; Soumaya,Mougou-Zerelli ^[1]

作者单位： Laboratory of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Teaching Hospital, Sousse, Tunisia. ^[1] Higher Institute of Biotechnology, Monastir University, Monastir, Tunisia. ^[2] Unité de Services Communs en Génétique Humaine, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia. ^[3] Pediatric Department, Farhat Hached University Teaching Hospital, Sousse, Tunisia. ^[4] Pediatric Department, Regional Hospital, Kairouan, Tunisia. ^[5] Laboratory of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Teaching Hospital, Sousse, Tunisia. mougousoumaya@yahoo.fr. ^[6] Unité de Services Communs en Génétique Humaine, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia. mougousoumaya@yahoo.fr. ^[7]

关键词 Array CGH FISH Hypospadias MSX1gene Wolf–Hirschhorn syndrome

DOI 10.1186/s13039-021-00531-8

PMID 33627176

发布时间 2021-02-28

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