These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

68 related articles for article (PubMed ID: 3225820)

  • 1. Prediction of consanguinity using human DNA fingerprints.
    Wells RA; Wonke B; Thein SL
    J Med Genet; 1988 Oct; 25(10):660-2. PubMed ID: 3225820
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prader-Willi syndrome in siblings, due to unbalanced translocation between chromosomes 15 and 22.
    Fernandez F; Berry C; Mutton D
    Arch Dis Child; 1987 Aug; 62(8):841-3. PubMed ID: 3662590
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The first observation of Hb D Punjab beta zero thalassaemia in an English family with 22 cases of unsuspected beta zero thalassaemia minor among its members.
    Worthington S; Lehmann H
    J Med Genet; 1985 Oct; 22(5):377-81. PubMed ID: 4078867
    [TBL] [Abstract][Full Text] [Related]  

  • 4. delta beta-Thalassaemia in Sicily: report of a case of double heterozygosity for A gamma delta beta-thalassaemia and A gamma G gamma delta beta-thalassaemia.
    Musumeci S; Romeo MA; Pizzarelli G; Schilirò G; Russo G
    J Med Genet; 1983 Feb; 20(1):73-5. PubMed ID: 6188831
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Chromosome 15 satellite enlargement and hereditary deafness].
    Zhuang J; Hu X; Zhang B
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1994; 29(4):225-7. PubMed ID: 7803123
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Study of a large Anglo-Saxon family with beta-thalassaemia trait.
    Raik E; Powell E; Gordon S
    Acta Haematol; 1976; 55(1):40-7. PubMed ID: 816138
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
    Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree].
    Jin Y; Hao X; Cheng X; Yang L; Chen Y; Xie H; Wang Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):296-9. PubMed ID: 27264807
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinico-genetic characteristics of thalassemia in Azerbaijan].
    Mutalimova AB; Nazarli AG
    Probl Gematol Pereliv Krovi; 1974 Oct; 19(10):14-8. PubMed ID: 4279402
    [No Abstract]   [Full Text] [Related]  

  • 11. Robertsonian translocation t dic (14p;22p) with regular trisomy 21: a possible interchromosomal effect?
    Farag TI; Krishna Murthy DS; Al-Awadi SA; Sundareshan TS; Ai-Othman SA; Mady SA; Redha MA
    Ann Genet; 1987; 30(3):189-92. PubMed ID: 2960263
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Hemoglobin H disease with a rare α-thalassemia gene mutation (--
    Yan SH; Lao KG; Fu KP; Gong FF; Wen XJ; Zhou WJ
    Nan Fang Yi Ke Da Xue Xue Bao; 2016 Aug; 36(9):1295-1298. PubMed ID: 27687668
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.
    Cianetti L; Care A; Sposi NM; Giampaolo A; Calandrini M; Petrini M; Massa A; Marinucci M; Mavilio F; Ceccanti M
    J Med Genet; 1984 Aug; 21(4):263-7. PubMed ID: 6208362
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency].
    Jin Y; Wang M; Wang Y; Yang X; Yang L; Xie Y; Xie H; Zhu L; Yu F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):16-20. PubMed ID: 24510554
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sperm aneuploidy and implications for genetic counseling in a pedigree of three t(1;3) balanced translocation carriers.
    Li LL; Dong Y; Wang RX; An N; Yun X; Liu RZ
    Genet Mol Res; 2015 May; 14(2):5003-9. PubMed ID: 25966275
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
    Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL
    Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
    Nazarenko SA; Nazarenko LP; Baranova VA
    Tsitol Genet; 1987; 21(6):434-7. PubMed ID: 3445362
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The frequency of consanguineous marriage among British Pakistanis.
    Darr A; Modell B
    J Med Genet; 1988 Mar; 25(3):186-90. PubMed ID: 3351906
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Duchenne type muscular dystrophy and consanguinity: difficulties in pedigree analysis.
    Aymé S; Pelissier JF; Garnier JM; Mattei JF; Giraud F
    J Med Genet; 1979 Oct; 16(5):393-5. PubMed ID: 513086
    [TBL] [Abstract][Full Text] [Related]  

  • 20. beta+ -Thalassemia intermedia. Genetic and biochemical study of a family including 3 cases.
    Philip T; Souillet G; Philippe N; Freycon F; Bektas S; Morlé L; Trabuchet G; Godet J
    Hum Hered; 1980; 30(5):324-30. PubMed ID: 6156119
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.