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154 related items for PubMed ID: 22253956
1. A Rare Case of Pericentric Inversion, Inv (21) (p12;q22) in Repeated Pregnancy Loss: A Case Report. Tayebi N, Khodaei H. Oman Med J; 2011 Nov; 26(6):441-3. PubMed ID: 22253956 [Abstract] [Full Text] [Related]
2. Subfertile couple with inv(2),inv(9) and 16qh+. Srebniak M, Wawrzkiewicz A, Wiczkowski A, Kaźmierczak W, Olejek A. J Appl Genet; 2004 Nov; 45(4):477-9. PubMed ID: 15523161 [Abstract] [Full Text] [Related]
3. Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population. Sismani C, Rapti SM, Iliopoulou P, Spring A, Neroutsou R, Lagou M, Robola M, Tsitsopoulos E, Kousoulidou L, Alexandrou A, Papaevripidou I, Theodosiou A, Syrrou M, Fuchs S, Hempel M, Huhle D, Liehr T, Ziegler M, Duesberg M, Velissariou V. J Hum Genet; 2020 Sep; 65(9):783-795. PubMed ID: 32398760 [Abstract] [Full Text] [Related]
4. Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports. Wan X, Li L, Liu Z, Fan Z, Yu L. J Med Case Rep; 2021 May 24; 15(1):270. PubMed ID: 34024271 [Abstract] [Full Text] [Related]
5. Familial pericentric and paracentric inversions of chromosome 1. Johnson DD, Dobyns WB, Gordon H, Dewald GW. Hum Genet; 1988 Aug 24; 79(4):315-20. PubMed ID: 3410456 [Abstract] [Full Text] [Related]
6. Clinical implications of chromosomal inversions. A pericentric inversion in No. 18 segregating in a family ascertained through an abnormal proband. Martin AO, Simpson JL, Deddish RB, Elias S. Am J Perinatol; 1983 Oct 24; 1(1):81-8. PubMed ID: 6680656 [Abstract] [Full Text] [Related]
7. Chromosome 9 Inversion: Pathogenic or Benign? A Comprehensive Systematic Review of all Clinical Reports. Mohsen-Pour N, Talebi T, Naderi N, Moghadam MH, Maleki M, Kalayinia S. Curr Mol Med; 2022 Oct 24; 22(5):385-400. PubMed ID: 34365947 [Abstract] [Full Text] [Related]
8. Impact of pericentric inversion of Chromosome 9 [inv (9) (p11q12)] on infertility. Mozdarani H, Meybodi AM, Karimi H. Indian J Hum Genet; 2007 Jan 24; 13(1):26-9. PubMed ID: 21957338 [Abstract] [Full Text] [Related]
9. The significance of pericentric inversions of chromosome 2. Djalali M, Steinbach P, Bullerdiek J, Holmes-Siedle M, Verschraegen-Spae MR, Smith A. Hum Genet; 1986 Jan 24; 72(1):32-6. PubMed ID: 3943862 [Abstract] [Full Text] [Related]
10. Pericentric inversions in man: personal experience and review of the literature. Kleczkowska A, Fryns JP, Van den Berghe H. Hum Genet; 1987 Apr 24; 75(4):333-8. PubMed ID: 3570287 [Abstract] [Full Text] [Related]
11. Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion. Ciuladaite Z, Preiksaitiene E, Utkus A, Kučinskas V. Cytogenet Genome Res; 2014 Apr 24; 144(2):109-13. PubMed ID: 25401700 [Abstract] [Full Text] [Related]
12. Subfertile couple with t(4;22)(q23;q11.2). Srebniak M, Popowska L, Wawrzkiewicz-Witkowska A, Tomaszewska A, Kazmierczak W. J Appl Genet; 2005 Apr 24; 46(3):333-6. PubMed ID: 16110194 [Abstract] [Full Text] [Related]
13. Fertility problems in males carrying an inversion of chromosome 10. Zhang X, Shi Q, Liu Y, Jiang Y, Yang X, Liu R, Zhang H. Open Med (Wars); 2021 Apr 24; 16(1):316-321. PubMed ID: 33681470 [Abstract] [Full Text] [Related]
14. Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine sampling. Demirhan O, Ozcan K, Taştemir D, Demir C, Tunç E, Solğun HA, Güzel AI. Fertil Steril; 2008 Jan 24; 89(1):228.e1-6. PubMed ID: 17880960 [Abstract] [Full Text] [Related]
15. Pericentric inversion of chromosom 12 [Inv (12) (p12q12)] associated with idiopathic azoospermia in one infertile Tunisian man. Ghorbel M, Baklouti-Gargouri S, ElGhazel H, Zribi N, Ben Abdallah F, Cherif M, Fakhfakh F, Saad A, Ammar-Keskes L. Biochem Biophys Res Commun; 2013 Mar 15; 432(3):472-4. PubMed ID: 23399567 [Abstract] [Full Text] [Related]
16. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. Daniel A, Hook EB, Wulf G. Am J Med Genet; 1989 May 15; 33(1):14-53. PubMed ID: 2750783 [Abstract] [Full Text] [Related]
17. A large pericentric inversion of human chromosome 8. Herva R, de la Chapelle A. Am J Hum Genet; 1976 May 15; 28(3):208-12. PubMed ID: 944528 [Abstract] [Full Text] [Related]
18. Pericentric inversion of chromosome 9 in prenatal diagnosis and infertility. Uehara S, Akai Y, Takeyama Y, Takabayashi T, Okamura K, Yajima A. Tohoku J Exp Med; 1992 Apr 15; 166(4):417-27. PubMed ID: 1502688 [Abstract] [Full Text] [Related]
19. Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers. Sutherland GR, Gardiner AJ, Carter RF. Clin Genet; 1976 Jul 15; 10(1):54-9. PubMed ID: 949865 [Abstract] [Full Text] [Related]
20. Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies. Atli EI, Atli E, Inan C, Varol GF, Mail C, Erbilen EA, Yalcintepe S, Demir S, Gurkan H. Taiwan J Obstet Gynecol; 2022 May 15; 61(3):504-509. PubMed ID: 35595446 [Abstract] [Full Text] [Related] Page: [Next] [New Search]