157 related articles for article (PubMed ID: 1519640)
1. Ullrich-Turner syndrome with unilateral agenesis of breast, nipple, and pectoralis major.
Cohen A; Lavagetto A; Romano C
Am J Med Genet; 1992 Sep; 44(1):11-2. PubMed ID: 1519640
[TBL] [Abstract][Full Text] [Related]
2. Bilateral Poland anomaly.
Karnak I; Tanyel FC; Tunçbilek E; Unsal M; Büyükpamukçu N
Am J Med Genet; 1998 Feb; 75(5):505-7. PubMed ID: 9489794
[TBL] [Abstract][Full Text] [Related]
3. Reply to correspondence from Shipkov and Anastassov--"Bilateral Poland anomaly: does it exist?".
Karnak I; Tanyel FC
Am J Med Genet A; 2003 Mar; 117A(3):310-1. PubMed ID: 12599202
[No Abstract] [Full Text] [Related]
4. Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18.
Franceschini P; Guala A; Camerano P; Franceschini D; Vardeu MP; Signorile F
Am J Med Genet; 1996 Mar; 62(1):26-8. PubMed ID: 8779320
[TBL] [Abstract][Full Text] [Related]
5. Ullrich-Turner syndrome with agenesis of the corpus callosum.
Kimura M; Nakajima M; Yoshino K
Am J Med Genet; 1990 Oct; 37(2):227-8. PubMed ID: 2248289
[TBL] [Abstract][Full Text] [Related]
6. Isodicentric X chromosome and mosaicism: report on two cases of 45,X/46,X,idic(Xq)/47,X,idic(Xq),idic(Xq) and review of the literature.
Melaragno MI; Fakih LM; Cernach MC; Maccagnan P
Am J Med Genet; 1993 Sep; 47(3):357-9. PubMed ID: 8135281
[TBL] [Abstract][Full Text] [Related]
7. Scalp-ear-nipple syndrome: additional manifestations.
Edwards MJ; McDonald D; Moore P; Rae J
Am J Med Genet; 1994 Apr; 50(3):247-50. PubMed ID: 8042668
[TBL] [Abstract][Full Text] [Related]
8. [Poland-Möbius syndrome associated with lacrimal punctal and canalicular agenesis].
Aydin A; Ayata A; Sabahyildizi M; Ersanli D
J Fr Ophtalmol; 2010 Feb; 33(2):119.e1-5. PubMed ID: 20061050
[TBL] [Abstract][Full Text] [Related]
9. Congenital absence of the breast.
Booth DH; Persaud TV
Anat Anz; 1984; 155(1-5):29-30. PubMed ID: 6721193
[TBL] [Abstract][Full Text] [Related]
10. 46,X,i(Xq)/47,XX,+13 mosaicism.
Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T
Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438
[TBL] [Abstract][Full Text] [Related]
11. Analysis of the SRY gene in a girl with 45,X/46,XY genotype.
Akbas E; Soylemez F; Hallioglu O; Polat S; Turkoz G
Genet Couns; 2009; 20(3):249-54. PubMed ID: 19852431
[TBL] [Abstract][Full Text] [Related]
12. Ullrich-Turner syndrome (45,X/46,X,i[Xq]) in a child with a familial inversion of chromosome 3.
Stine SB; Clark CE; Telfer MA; Casey PA; Cowell HR
Am J Med Genet; 1982 May; 12(1):57-62. PubMed ID: 7091197
[TBL] [Abstract][Full Text] [Related]
13. [Poland syndrome--clinical study].
Vasileva P; Radev R
Akush Ginekol (Sofiia); 2007; 46 Suppl 2():16-9. PubMed ID: 18173004
[TBL] [Abstract][Full Text] [Related]
14. Ullrich-Turner syndrome and neurofibromatosis-1.
Schorry EK; Lovell AM; Milatovich A; Saal HM
Am J Med Genet; 1996 Dec; 66(4):423-5. PubMed ID: 8989459
[TBL] [Abstract][Full Text] [Related]
15. Poland syndrome: description of an atypical variant.
Ferraro GA; Perrotta A; Rossano F; D'Andrea F
Aesthetic Plast Surg; 2005; 29(1):32-3. PubMed ID: 15759092
[TBL] [Abstract][Full Text] [Related]
16. Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.
Chen CP; Lin SP; Tsai FJ; Chern SR; Wang W
Fertil Steril; 2008 Jun; 89(6):1826.e5-7. PubMed ID: 17953951
[TBL] [Abstract][Full Text] [Related]
17. Poland syndrome.
Urschel HC
Semin Thorac Cardiovasc Surg; 2009; 21(1):89-94. PubMed ID: 19632568
[TBL] [Abstract][Full Text] [Related]
18. X-inactivation pattern in an Ullrich-Turner syndrome patient with a small ring X and normal intelligence.
Zenger-Hain JL; Wiktor A; Goldman J; Van Dyke DL; Weiss L
Am J Med Genet; 1993 Sep; 47(4):490-3. PubMed ID: 8256812
[TBL] [Abstract][Full Text] [Related]
19. Ullrich-Turner syndrome in monozygotic twins.
Al-Awadi SA; Cuschieri A; Farag TI; Naguib K; Teebi AS; Al-Othman SA; Bahig AH
Am J Med Genet; 1983 Aug; 15(4):537-42. PubMed ID: 6684396
[TBL] [Abstract][Full Text] [Related]
20. Ullrich-Turner syndrome in mother and daughter: prenatal diagnosis of a 46,X,del(X)(p21) offspring from a 45,X mother with low-level mosaicism for the del(X)(p21) in one ovary.
Varela M; Shapira E; Hyman DB
Am J Med Genet; 1991 Jun; 39(4):411-2. PubMed ID: 1877618
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
