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 *

137 related articles for article (PubMed ID: 7083613)

  • 81. Molecular characterisation of a 3.5 Mb interstitial 14q deletion in a child with several phenotypic anomalies.
    Petek E; Plecko-Startinig B; Windpassinger C; Egger H; Wagner K; Kroisel PM
    J Med Genet; 2003 Apr; 40(4):e47. PubMed ID: 12676920
    [No Abstract]   [Full Text] [Related]  

  • 82. Deletion in chromosome region 22q11 in a child with CHARGE association.
    Devriendt K; Swillen A; Fryns JP
    Clin Genet; 1998 May; 53(5):408-10. PubMed ID: 9660062
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23.
    Voullaire LE; Webb GC; Leversha MA
    Hum Genet; 1987 Jun; 76(2):202-4. PubMed ID: 3610150
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
    Taysi K; Strauss AW; Yang V; Padmalatha C; Marshall RE
    Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Monosomy 22 with mosaicism.
    Moghe MS; Patel ZM; Peter JJ; Ambani LM
    J Med Genet; 1981 Feb; 18(1):71-3. PubMed ID: 7253004
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Deletion 1q42.3----qter in a girl with psychomotoric retardation and multiple dysmorphisms.
    Kausch K; Köhler J; Schmid M
    Ann Genet; 1988; 31(3):193-4. PubMed ID: 3265611
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Developmental abnormalities associated with long arm deletion of chromosome No. 6.
    Bartoshesky L; Lewis MB; Pashayan HM
    Clin Genet; 1978 Jan; 13(1):68-71. PubMed ID: 624189
    [TBL] [Abstract][Full Text] [Related]  

  • 88. A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.
    Genuardi M; Calvieri F; Tozzi C; Coslovi R; Neri G
    Clin Dysmorphol; 1994 Oct; 3(4):292-6. PubMed ID: 7894733
    [TBL] [Abstract][Full Text] [Related]  

  • 89. A case of a female infant with simultaneous occurrence of de novo terminal deletions on chromosome 14q and 20p.
    Uehara S; Akai Y; Takeyama Y; Okamura K; Takabayashi T; Yajima A; Natsui M; Nakai H
    Clin Genet; 1993 Jan; 43(1):28-33. PubMed ID: 8179640
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
    Descartes M; Keppler-Noreuil K; Knops J; Longshore JW; Finley WH; Carroll AJ
    Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Interstitial deletion of chromosome 13 and associated congenital anomalies.
    Nichols WW; Miller RC; Hoffman E; Albert D; Weichselbaum RR; Nove J; Little JB
    Hum Genet; 1979 Nov; 52(2):169-73. PubMed ID: 511172
    [TBL] [Abstract][Full Text] [Related]  

  • 92. A report of a child with a deletion (9)(q34.3): a recognisable phenotype?
    Ayyash H; Mueller R; Maltby E; Horsfield P; Telford N; Tyler R
    J Med Genet; 1997 Jul; 34(7):610-2. PubMed ID: 9222977
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Ring chromosome 4.
    McDermott A; Voyce MA; Romain D
    J Med Genet; 1977 Jun; 14(3):228-32. PubMed ID: 881718
    [TBL] [Abstract][Full Text] [Related]  

  • 94. 46,XY/46,XX blood chimerism with severe central nervous system defect and multiple congenital malformations.
    Lieber C; Bordiuk J; Desposito F
    Am J Med Genet; 1986 Mar; 23(3):833-6. PubMed ID: 3953679
    [No Abstract]   [Full Text] [Related]  

  • 95. Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype.
    Overhauser J; Golbus MS; Schonberg SA; Wasmuth JJ
    Am J Hum Genet; 1986 Jul; 39(1):1-10. PubMed ID: 3752077
    [TBL] [Abstract][Full Text] [Related]  

  • 96. On the use of distribution-functions to describe and classify chromosome density-profiles.
    van den Berg HT; Habbema JD; de France HF; Bakker HK; de Vries GA
    Comput Biol Med; 1979; 9(1):11-20. PubMed ID: 421432
    [No Abstract]   [Full Text] [Related]  

  • 97. Human chromosomal heteromorphisms in American blacks. IV. Intensity variation in centromeric regions of chromosomes 3 and 4.
    Verma RS; Dosik H
    Can J Genet Cytol; 1981; 23(2):315-20. PubMed ID: 7296354
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Piebald trait in a retarded child with interstitial deletion of chromosome 4.
    Lacassie Y; Thurmon TF; Tracy MC; Pelias MZ
    Am J Hum Genet; 1977 Nov; 29(6):641-2. PubMed ID: 930930
    [No Abstract]   [Full Text] [Related]  

  • 99. Genomic imprinting for pathologists.
    Berry CL
    Virchows Arch A Pathol Anat Histopathol; 1991; 419(5):363-4. PubMed ID: 1836291
    [No Abstract]   [Full Text] [Related]  

  • 100. Genetic markers in individuals with a 5p- karyotype.
    Fenger K; Møhl IA
    Clin Genet; 1979 Jul; 16(1):58-9. PubMed ID: 477016
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.