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 *

119 related articles for article (PubMed ID: 1036373)

  • 21. On the deletion 4p16 Wolf-Hirschhorn syndrome.
    Rivas F; Hernandez A; Nazara Z; Fragoso R; Olivares N; Rolon A; Cantu JM
    Ann Genet; 1979; 22(4):228-31. PubMed ID: 317787
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
    Yamagishi H; Ishii C; Maeda J; Kojima Y; Matsuoka R; Kimura M; Takao A; Momma K; Matsuo N
    Am J Med Genet; 1998 Jul; 78(4):319-21. PubMed ID: 9714432
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Monozygotic twins discordant for rubinstein-taybi syndrome.
    Kajii T; Hagiwara K; Tsukahara M; Nakajima H; Fukuda Y
    J Med Genet; 1981 Aug; 18(4):312-4. PubMed ID: 7196955
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Duplication of region 2q31 leads to 2qter in a family with 2/9 translocation.
    Howard-Peebles PN; Goldsmith JP
    Hum Hered; 1980; 30(2):84-8. PubMed ID: 7358400
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Skeletal changes in Wolf's syndrome (4p--) and in Klinefelter quadrisomy (author's transl)].
    Montanelli C; Lucchi A; Canini R; Boriani F; Pangia G; De Florio L
    Radiol Med; 1979 Nov; 65(11):807-12. PubMed ID: 554201
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 4p- phenotype in an infant with t(4p-;19p or q+)mat translocation.
    Neu RL; Shott RJ; Gardner LI
    Am J Dis Child; 1975 Mar; 129(3):363-5. PubMed ID: 1121967
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Ring chromosome 4 in twins].
    Giuffrè L; Cammarata M; Corsello G; Benigno V; Graziano L; Roccella F; Balsamo V
    Pediatr Med Chir; 1987; 9(3):349-50. PubMed ID: 3671134
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Monozygotic twins with trisomy 18: a report of discordant phenotype.
    Schlessel JS; Brown WT; Lysikiewicz A; Schiff R; Zaslav AL
    J Med Genet; 1990 Oct; 27(10):640-2. PubMed ID: 2246775
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB; Stevens CA
    Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interstitial deletion of the short arm of chromosome 4.
    Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The 18p- syndrome. Report of five cases.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Concordant congenital malformations in twins with inherited translocation: t(9p--;13q+).
    Sekhon GS; Taysi K
    Hum Genet; 1979 Sep; 50(3):271-6. PubMed ID: 489011
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinicopathologic conference: dup(10q),del(12p) in one abnormal, dizygotic twin infant of a t(10;12) (q22.1;p13.3) mother.
    Juberg RC; Christopher CR; Alvira MM; Gilbert EF
    Am J Med Genet; 1984 Jun; 18(2):201-13. PubMed ID: 6465197
    [No Abstract]   [Full Text] [Related]  

  • 35. The campomelic syndrome in a singleton and monozygotic twins.
    Moedjono SJ; Crandall BF; Sparkes RS; Feldman GM; Austin GE; Perry S
    Clin Genet; 1980 Dec; 18(6):397-401. PubMed ID: 7192615
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Balanced rearrangement of chromosomes 2, 5, and 13 in a family with duplication 5q and fetal loss.
    Evans MI; White BJ; Kent SG; Levine MA; Levin SW; Larsen JW
    Am J Med Genet; 1984 Dec; 19(4):783-90. PubMed ID: 6517101
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Acute lymphoblastic leukemia in adult identical twins.
    Hecht T; Henke M; Schempp W; Bross KJ; Löhr GW
    Blut; 1988 Jun; 56(6):261-4. PubMed ID: 3289633
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

  • 39. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 40. Penetrance and low concordance in monozygotic twins in disease: are they the results of alterations in somatic genomes?
    Kastern W; Kryspin-Sorensen I
    Mol Reprod Dev; 1988; 1(1):63-75. PubMed ID: 2856085
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.