124 related articles for article (PubMed ID: 1951429)
1. Partial duplication of Xp: a case report and review of previously reported cases.
Wyandt HE; Bugeau-Michaud L; Skare JC; Milunsky A
Am J Med Genet; 1991 Sep; 40(3):280-3. PubMed ID: 1951429
[TBL] [Abstract][Full Text] [Related]
2. A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family.
Karaman B; Wollnik B; Ermiş H; Yüksel-Apak M; Başaran S
Prenat Diagn; 2003 Apr; 23(4):336-9. PubMed ID: 12673642
[TBL] [Abstract][Full Text] [Related]
3. De novo duplication xq22-q23 in a girl with short stature and gonadal dysgenesis.
Correa-Cerro L; Garcia-Cruz D; Ruiz MX; Sanchez-Corona J
Ann Genet; 1999; 42(1):41-4. PubMed ID: 10214506
[TBL] [Abstract][Full Text] [Related]
4. Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short stature.
Abulhasan SJ; Teebi AS; Zaki M; Hammad I; Al-Awadi SA; Krishna Murthy DS
Ann Genet; 1990; 33(4):234-8. PubMed ID: 2095706
[TBL] [Abstract][Full Text] [Related]
5. Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome.
Burégio-Frota P; Valença L; Leal GF; Duarte AR; Bispo-Brito AV; Soares-Ventura EM; Marques-Salles TJ; Nogueira MT; Muniz MT; Silva ML; Hunstig F; Liehr T; Santos N
Genet Mol Res; 2010 Apr; 9(2):780-4. PubMed ID: 20449811
[TBL] [Abstract][Full Text] [Related]
6. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
[TBL] [Abstract][Full Text] [Related]
7. Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.
Matsuo M; Muroya K; Kosaki K; Ishii T; Fukushima Y; Anzo M; Ogata T
Am J Med Genet; 1999 Sep; 86(1):44-50. PubMed ID: 10440827
[TBL] [Abstract][Full Text] [Related]
8. Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
Sarda P; Lefort G; Devaux P; Humeau C; Rieu D
Ann Genet; 1992; 35(2):117-20. PubMed ID: 1524409
[TBL] [Abstract][Full Text] [Related]
9. Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.
Giglio S; Pirola B; Arrigo G; Dagrada P; Bardoni B; Bernardi F; Russo G; Argentiero L; Forabosco A; Carrozzo R; Zuffardi O
Eur J Hum Genet; 2000 Jan; 8(1):63-70. PubMed ID: 10713889
[TBL] [Abstract][Full Text] [Related]
10. [Chromosome X with partial long arm deletion. Three cases].
Teyssier M; Charrin C
J Gynecol Obstet Biol Reprod (Paris); 1992; 21(4):413-7. PubMed ID: 1624728
[TBL] [Abstract][Full Text] [Related]
11. [Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].
Reichenbach H; Holland H; Thamm B; Theile T
Kinderarztl Prax; 1993 Oct; 61(7-8):291-5. PubMed ID: 8271681
[TBL] [Abstract][Full Text] [Related]
12. [A second case of (de novo) paracentric inversion of the short arm of the X chromosome].
Dahoun S
Ann Genet; 1990; 33(1):52-5. PubMed ID: 2195983
[TBL] [Abstract][Full Text] [Related]
13. Molecular cytogenetic characterization of a case of primary amenorrhea with intrachromosomal triplication of the X chromosome q arm.
Ocak Z; Surucu R
Genet Couns; 2012; 23(2):297-304. PubMed ID: 22876590
[TBL] [Abstract][Full Text] [Related]
14. Growth hormone deficiency and empty sella syndrome in a boy with dup(X) (q13.3----q21.2).
Yokoyama Y; Narahara K; Tsuji K; Moriwake T; Kanzaki S; Murakami M; Namba H; Ninomiya S; Higuchi J; Seino Y
Am J Med Genet; 1992 Mar; 42(5):660-4. PubMed ID: 1632433
[TBL] [Abstract][Full Text] [Related]
15. Short stature in a mother and daughter with terminal deletion of Xp22.3.
Schwinger E; Kirschstein M; Greiwe M; Konermann T; Orth U; Gal A
Am J Med Genet; 1996 May; 63(1):239-42. PubMed ID: 8723116
[TBL] [Abstract][Full Text] [Related]
16. The origin of inverted tandem duplications, and phenotypic effects of tandem duplication of the X chromosome long arm.
Van Dyke DL; Miller MJ; Weiss L
Am J Med Genet; 1983 Jul; 15(3):441-50. PubMed ID: 6881211
[TBL] [Abstract][Full Text] [Related]
17. A 48,XXXX female with absence of ovaries.
Collen RJ; Falk RE; Lippe BM; Kaplan SA
Am J Med Genet; 1980; 6(4):275-8. PubMed ID: 7211945
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.
Tihy F; Lemyre E; Lemieux N; Dallaire L
Am J Med Genet; 1999 Dec; 87(4):302-5. PubMed ID: 10588834
[TBL] [Abstract][Full Text] [Related]
20. Ullrich-Turner syndrome associated with interstitial deletion of Xp11.4 leads to p22.31.
Wilson MG; Modebe O; Towner JW; Frasier SD; Lin MS
Am J Med Genet; 1983 Mar; 14(3):567-76. PubMed ID: 6859107
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
