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Journal Abstract Search

243 related items for PubMed ID: 6974525

  • 1. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
    Yu CW, Chen H, Baucum RW, Hand AM.
    Ann Genet; 1981; 24(3):158-61. PubMed ID: 6974525
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  • 2. [Syndrome of terminal deletion of the long arm of chromosome 4. Apropos of a personal case with a review of the literature].
    Frappaz D, Bourgeois J, Berthier JC, Laurent C, Bethenod M.
    Pediatrie; 1983 Jun; 38(4):261-70. PubMed ID: 6353348
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  • 6. Deletion of a portion of the long arm of chromosome 6.
    Goldberg R, Fish B, Ship A, Shprintzen RJ.
    Am J Med Genet; 1980 Jun; 5(1):73-80. PubMed ID: 7395903
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  • 7. Deletions of different segments of the long arm of chromosome 4.
    Mitchell JA, Packman S, Loughman WD, Fineman RM, Zackai E, Patil SR, Emanual B, Bartley JA, Hanson JW.
    Am J Med Genet; 1981 Jun; 8(1):73-89. PubMed ID: 7246608
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  • 8. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
    Back E, Hertel C, Vogel W, Bettecken F, Thiesen M.
    Ann Genet; 1977 Dec; 20(4):294-6. PubMed ID: 305761
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  • 11. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.
    Boles RG, Pober BR, Gibson LH, Willis CR, McGrath J, Roberts DJ, Yang-Feng TL.
    Am J Med Genet; 1995 Jan 16; 55(2):155-60. PubMed ID: 7717414
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  • 12. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
    Wang TH, Johnston K, Hsieh CL, Dennery PA.
    Am J Med Genet; 1994 Feb 15; 49(4):399-401. PubMed ID: 8160733
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  • 13. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
    Chitayat D, Babul R, Silver MM, Jay V, Teshima IE, Babyn P, Becker LE.
    Am J Med Genet; 1996 Jan 02; 61(1):45-8. PubMed ID: 8741917
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  • 14. Interstitial deletion of long arm of chromosome 13.
    Carnevale A, Frias S, Alcantar R.
    Ann Genet; 1984 Jan 02; 27(1):49-52. PubMed ID: 6609673
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  • 15. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL, Roberson J, Van Dyke DL, Weiss L.
    Am J Med Genet; 1993 Jun 01; 46(4):438-40. PubMed ID: 7689299
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  • 17. [Terminal deletion of the long arm of chromosome 4:46,XY, del (4) (q31.3----qter: a case after in vitro fertilization].
    Lizarraga Azparren MA, Escudero Jiménez F, Lasarte Iradi JR, Sojo Aguirre A, Aramburu Bardesi N, Labayru Echebarría M, Tejada MI, Centeno Monterrubio C.
    An Esp Pediatr; 1991 May 01; 34(5):404-6. PubMed ID: 1883118
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  • 18. Multiple congenital anomalies, thymic dysplasia, severe congenital heart disease, and oligosyndactyly with a deletion of the short arm of chromosome 5.
    Taylor MJ, Josifek K.
    Am J Med Genet; 1981 May 01; 9(1):5-11. PubMed ID: 6264787
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  • 19. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
    Dobyns WB, Dewald GW, Carlson RO, Mair DD, Michels VV.
    Am J Med Genet; 1985 Sep 01; 22(1):125-34. PubMed ID: 3901750
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  • 20. Interstitial deletion of the long arm of chromosome 4 [del(4)(q21.22q23)] and a liver tumor.
    Suwa K, Momoi MY, Yamagata T, Mori Y.
    Am J Med Genet; 1998 Jul 07; 78(3):291-3. PubMed ID: 9677069
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