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 *

75 related articles for article (PubMed ID: 1196721)

  • 1. [Translocation of group D chromosomes in a child with a congenital syndrome of neuromyodysplasia and mental retardation].
    Traczyńska-Kubin H; Czerski P; Rogóyski A; Stolarska A
    Pediatr Pol; 1975 Dec; 50(12):1485-7. PubMed ID: 1196721
    [No Abstract]   [Full Text] [Related]  

  • 2. [Clinical case of tandem translocation between chromosomes 13 and 15].
    Badalian LO; Arkhipov BA; Malygina NA; Patrukhin AS; Lysov VL
    Tsitol Genet; 1985; 19(4):304-8. PubMed ID: 4049521
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Apropos of a translocation of a part of the long arms of a chromosome 5 on the long arms of a chromosome of the D group (Bq-, Dq+)].
    Beauvais P; Rumpler Y; Ruch JV; Dreyfus J; Haeberle C
    Arch Fr Pediatr; 1969; 26(6):695-704. PubMed ID: 5802061
    [No Abstract]   [Full Text] [Related]  

  • 4. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA; Mikel'saar AV; Mikel'saar RV
    Sov Genet; 1974 Jun; 8(5):651-7. PubMed ID: 4413436
    [No Abstract]   [Full Text] [Related]  

  • 5. [The "Copenhagen chromosome" (syndrome of the small metacentric extra-chromosome)].
    Haberlandt W
    Arztl Forsch; 1971 Jul; 25(7):218-23. PubMed ID: 5109598
    [No Abstract]   [Full Text] [Related]  

  • 6. [Dysmorphic syndrome and D-D translocation. Coincidence or tight consequence?].
    Giovannucci ML
    Riv Clin Pediatr; 1969; 82():445-51. PubMed ID: 5405501
    [No Abstract]   [Full Text] [Related]  

  • 7. [A patient with ring chromosome 13].
    Hammond A; Bijlsma JB
    Ned Tijdschr Geneeskd; 1981 May; 125(19):752-5. PubMed ID: 7242723
    [No Abstract]   [Full Text] [Related]  

  • 8. The KOP translocation.
    Pallister PD; Opitz JM
    Birth Defects Orig Artic Ser; 1978; 14(6C):133-46. PubMed ID: 569514
    [No Abstract]   [Full Text] [Related]  

  • 9. [Mosaic variant of the translocation form of syndrome 18q-].
    Badalian LO; Dement'eva GM; Malygina NA; Mutovin GR; Petrukhin AS
    Genetika; 1981; 17(10):1867-71. PubMed ID: 7198075
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A clinical syndrome associated with dup(5p).
    Carnevale A; Hernández M; Limón-Toledo I; Frías S; Castillo J; Del Castillo V
    Am J Med Genet; 1982 Nov; 13(3):277-83. PubMed ID: 7180873
    [No Abstract]   [Full Text] [Related]  

  • 11. Silver staining of the supernumerary chromosome in the cat-eye syndrome.
    Petit P; Godart S; Fryns JP
    Ann Genet; 1980; 23(2):114-6. PubMed ID: 6156636
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transmission of ring 14 chromosome from mother to two sons.
    Matalon R; Supple P; Wyandt H; Rosenthal IM
    Am J Med Genet; 1990 Aug; 36(4):381-5. PubMed ID: 2202211
    [TBL] [Abstract][Full Text] [Related]  

  • 13. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
    Chitayat D; Fagerstrom CL; Kalousek DK; Rootman J; Taylor GP; Hall JG
    Am J Med Genet; 1989 Jan; 32(1):36-41. PubMed ID: 2495721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
    Curry CJ; Ying KL; O'Lague P; Tsai J
    Birth Defects Orig Artic Ser; 1982; 18(3B):275-86. PubMed ID: 7139110
    [No Abstract]   [Full Text] [Related]  

  • 16. [Chromosome translocation D/D--incidence and importance].
    Neuhäuser G
    Hippokrates; 1975 Jun; 46(2):240-2. PubMed ID: 129443
    [No Abstract]   [Full Text] [Related]  

  • 17. [13q+ chromosome due to a probable translocation of a supernumerary Y].
    Gilgenkrantz S; Pierson M; Mauuary G
    Ann Genet; 1973 Sep; 16(3):167-72. PubMed ID: 4543205
    [No Abstract]   [Full Text] [Related]  

  • 18. [States of fragility of chromosome 7 in man].
    Bugnon C; Bresson JL
    Bull Assoc Anat (Nancy); 1976 Sep; 60(170):469-79. PubMed ID: 1028444
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
    Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
    Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
    Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
    Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.