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Journal Abstract Search

83 related items for PubMed ID: 6606378

  • 1. [Distal 1q monosomy. 2 new cases and description of the syndrome].
    Turleau C, de Grouchy J, Frézal J, Richardet JM.
    Ann Genet; 1983; 26(3):161-4. PubMed ID: 6606378
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  • 2. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP, Heck LJ, Carter GA, Flom JO.
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
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  • 3. [Trisomy 10q24--10qter].
    Dutrillaux B, Laurent C, Bernasconi S, Lejeune J.
    Ann Genet; 1975 Dec; 18(4):217-22. PubMed ID: 1083188
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  • 6. Terminal deletion 1q43 in a newborn with hydrocephalus.
    Ribeiro MC, Brunoni D.
    Ann Genet; 1987 Dec; 30(2):126-8. PubMed ID: 3499845
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  • 7. [Distal 14q trisomy].
    Turleau C, de Grouchy J, Chavin-Colin F, Denavit MF, Le Touzé P.
    Ann Genet; 1983 Dec; 26(3):165-70. PubMed ID: 6606379
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  • 8. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson EC, Holden JJ, Lewis ME, Rajcan-Separovic E.
    Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
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  • 11. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
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  • 13. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML, Pai GS, Wilkes B, Lebel RR.
    Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200
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  • 14. Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
    Chen CP, Lin SP, Lee CC, Town DD, Wang W.
    Genet Couns; 2006 Aug 15; 17(3):301-6. PubMed ID: 17100198
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  • 15. Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome.
    Reish O, Berry SA, Hirsch B.
    Am J Med Genet; 1995 Dec 04; 59(4):467-75. PubMed ID: 8585567
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  • 18. [Facial deformity associated with acquired immunodeficiency syndrome (AIDS). Report of two cases].
    Castillo Ariza M, Almonte Paulino R, Ariza Castillo F.
    Arch Domin Pediatr; 1988 Dec 04; 24(3):97-101. PubMed ID: 12343554
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  • 19. The 4P-syndrome. Case description and literature review.
    Moretti P, Ferrari M, Di Battista S, Di Battista C.
    Minerva Pediatr; 2001 Feb 04; 53(1):23-8. PubMed ID: 11309539
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  • 20. Duplication dup(1)(q41q44) defined by fluorescence in situ hybridization: delineation of the 'trisomy 1q42-->qter syndrome'.
    Coccé MC, Villa O, Obregon MG, Salido M, Barreiro C, Solé F, Gallego MS.
    Cytogenet Genome Res; 2007 Feb 04; 118(1):84-6. PubMed ID: 17901705
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