136 related articles for article (PubMed ID: 8162159)
1. What are the indications for prenatal diagnosis in the androgen insensitivity syndrome? Facing clinical heterogeneity of phenotypes for the same genotype.
Morel Y; Mebarki F; Forest MG
Eur J Endocrinol; 1994 Apr; 130(4):325-6. PubMed ID: 8162159
[No Abstract] [Full Text] [Related]
2. Prenatal diagnosis of androgen insensitivity syndrome.
Bianca S; Cataliotti A; Bartoloni G; Torrente I; Barrano B; Boemi G; Lo Presti M; Indaco L; Barone C; Ettore G
Fetal Diagn Ther; 2009; 26(3):167-9. PubMed ID: 19844078
[TBL] [Abstract][Full Text] [Related]
3. Androgen insensitivity syndrome: in utero diagnosis by four-dimensional sonography and amniotic fluid karyotype.
Bonilla-Musoles F; Kushner-Dávalos L; Raga F; Machado LE; Osborne NG
J Clin Ultrasound; 2006 Jan; 34(1):30-2. PubMed ID: 16353232
[TBL] [Abstract][Full Text] [Related]
4. Complete Androgen Insensitivity Syndrome: A Rare Case of Prenatal Diagnosis.
Coelho ML; Soares E; Freixo M; Brandão P; Marinho C; Rocha J; Rodrigues G
Rev Bras Ginecol Obstet; 2021 Sep; 43(9):710-712. PubMed ID: 34670306
[TBL] [Abstract][Full Text] [Related]
5. Early diagnosis of androgen insensitivity syndrome with cell-free fetal DNA screening: A case report.
Miller AS; Singh TA
Int J Gynaecol Obstet; 2024 Feb; 164(2):797-798. PubMed ID: 37922216
[No Abstract] [Full Text] [Related]
6. Molecular prenatal exclusion of familial partial androgen insensitivity (Reifenstein syndrome).
Lumbroso S; Lobaccaro JM; Belon C; Amram S; Bachelard B; Garandeau P; Sultan C
Eur J Endocrinol; 1994 Apr; 130(4):327-32. PubMed ID: 7909256
[TBL] [Abstract][Full Text] [Related]
7. Genotype versus phenotype in families with androgen insensitivity syndrome.
Boehmer AL; Brinkmann O; Brüggenwirth H; van Assendelft C; Otten BJ; Verleun-Mooijman MC; Niermeijer MF; Brunner HG; Rouwé CW; Waelkens JJ; Oostdijk W; Kleijer WJ; van der Kwast TH; de Vroede MA; Drop SL
J Clin Endocrinol Metab; 2001 Sep; 86(9):4151-60. PubMed ID: 11549642
[TBL] [Abstract][Full Text] [Related]
8. Prenatal Diagnosis of Twin Fetuses with a Novel AR Gene Mutation in a Chinese Family of Complete Androgen Insensitivity Syndrome.
Wu W; Geng Q; Liu Y; Xu Z; Li P; Xie J
Fetal Pediatr Pathol; 2017 Dec; 36(6):432-436. PubMed ID: 29206494
[TBL] [Abstract][Full Text] [Related]
9. Mutation analysis of androgen receptor gene: multiple uses for a single test.
Shojaei A; Behjati F; Ebrahimzadeh-Vesal R; Razzaghy-Azar M; Derakhshandeh-Peykar P; Izadi P; Kajbafzadeh AM; Dowlatih MA; Karami F; Tavakkoly-Bazzaz J
Gene; 2014 Dec; 552(2):234-8. PubMed ID: 25241384
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of androgen insensitivity syndrome using cell-free fetal DNA testing.
Zilberman D; Parikh LI; Skinner M; Landy HJ
Ultrasound Obstet Gynecol; 2015 Jan; 45(1):114-5. PubMed ID: 25291542
[No Abstract] [Full Text] [Related]
11. Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis.
Fogu G; Bertini V; Dessole S; Bandiera P; Campus PM; Capobianco G; Sanna R; Soro G; Montella A
Arch Gynecol Obstet; 2004 May; 269(4):266-9. PubMed ID: 12898143
[TBL] [Abstract][Full Text] [Related]
12. Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene.
Lobaccaro JM; Belon C; Lumbroso S; Olewniczack G; Carré-Pigeon F; Job JC; Chaussain JL; Toublanc JE; Sultan C
Clin Endocrinol (Oxf); 1994 Mar; 40(3):297-302. PubMed ID: 7910529
[TBL] [Abstract][Full Text] [Related]
13. [Androgen insensitivity syndrome].
Giwercman YL; Svensson J
Tidsskr Nor Laegeforen; 2008 Feb; 128(5):581-5. PubMed ID: 18311203
[TBL] [Abstract][Full Text] [Related]
14. Androgen insensitivity syndrome (AIS): emotional reactions of parents and adult patients to the clinical diagnosis of AIS and its confirmation by androgen receptor gene mutation analysis.
Slijper FM; Frets PG; Boehmer AL; Drop SL; Niermeijer MF
Horm Res; 2000; 53(1):9-15. PubMed ID: 10965214
[TBL] [Abstract][Full Text] [Related]
15. Androgen insensitivity syndrome: clinical features and molecular defects.
Galani A; Kitsiou-Tzeli S; Sofokleous C; Kanavakis E; Kalpini-Mavrou A
Hormones (Athens); 2008; 7(3):217-29. PubMed ID: 18694860
[TBL] [Abstract][Full Text] [Related]
16. [Testicular feminization syndrome associated with acute hydramnios: apropos of 1 case].
Jemmali M; Recktenwald JC
J Gynecol Obstet Biol Reprod (Paris); 2000 Dec; 29(8):797-800. PubMed ID: 11139718
[TBL] [Abstract][Full Text] [Related]
17. [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].
Soriano Guillén L; Muñoz Calvo MT; Martinez Pérez J; Pozo Román J; Martín Sobrino MA; González Medeiro I; Argente Oliver J
An Esp Pediatr; 2002 Apr; 56(4):347-52. PubMed ID: 11927080
[TBL] [Abstract][Full Text] [Related]
18. Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome.
Cheikhelard A; Morel Y; Thibaud E; Lortat-Jacob S; Jaubert F; Polak M; Nihoul-Fekete C
J Urol; 2008 Oct; 180(4):1496-501. PubMed ID: 18710728
[TBL] [Abstract][Full Text] [Related]
19. Preimplantation and prenatal genetic diagnosis for androgen insensitivity syndrome resulting from a novel deletion/insertion mutation.
Ye Y; Cong P; Yu P; Qi M; Jin F
Clin Genet; 2012 Sep; 82(3):295-6. PubMed ID: 22332610
[No Abstract] [Full Text] [Related]
20. [Androgen insensitivity syndrome. Clinical features and molecular genetics].
Sólyom J; Scheiber D; Fekete G
Orv Hetil; 2001 Aug; 142(31):1659-65. PubMed ID: 11556259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]