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25 in total

1. Mucociliary function, ciliary ultrastructure, and ciliary orientation in Young's syndrome.

Authors: R de Iongh; A Ing; J Rutland
Journal: Thorax Date: 1992-03 Impact factor: 9.139

Review 2. Sonographic findings of the genital tract in boys with cystic fibrosis.

Authors: Valeria Rathaus; Miriam Werner; Enrique Freud; Meir Mei-Zahav; Huda Mussaffi; Hanna Blau
Journal: Pediatr Radiol Date: 2005-12-02

3. Identification of a novel mutation in CFTR gene exon 8 (L375F) in a CUAVD phenotype.

Authors: P Jézéquel; B Chauvel; A Le Treut; J Y Le Gall; V David; D Le Lannou; M Blayau
Journal: Hum Genet Date: 1996-04 Impact factor: 4.132

4. CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesicles.

Authors: D Meschede; B Dworniczak; H M Behre; S Kliesch; M Claustres; E Nieschlag; J Horst
Journal: Am J Hum Genet Date: 1997-11 Impact factor: 11.025

5. CFTR gene variant for patients with congenital absence of vas deferens.

Authors: J Zielenski; P Patrizio; M Corey; B Handelin; D Markiewicz; R Asch; L C Tsui
Journal: Am J Hum Genet Date: 1995-10 Impact factor: 11.025

Review 6. Male hypogonadism.

Authors: W D Odell; R S Swerdloff
Journal: West J Med Date: 1976-06

Genital abnormalities in male patients with cystic fibrosis.

1. Mucociliary function, ciliary ultrastructure, and ciliary orientation in Young's syndrome.

Review 2. Sonographic findings of the genital tract in boys with cystic fibrosis.

3. Identification of a novel mutation in CFTR gene exon 8 (L375F) in a CUAVD phenotype.

4. CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesicles.

5. CFTR gene variant for patients with congenital absence of vas deferens.

Review 6. Male hypogonadism.

7. Some aspects of immunity in patients with cystic fibrosis.

8. Urogenital abnormalities in male children with cystic fibrosis.

9. Assessing the Disease-Liability of Mutations in CFTR.

Review 10. Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality.