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 *

219 related articles for article (PubMed ID: 939548)

  • 21. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J; Plaza J; Geán E
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two cases of an abnormal short arm of chromosome 8 (8p+) associated with mental retardation.
    Hongell K; Knuutila S; Westermarck T
    Clin Genet; 1978 Feb; 13(2):237-40. PubMed ID: 627113
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mental retardation and congenital malformations associated with a ring chromosome 6.
    Fried K; Rosenblatt M; Mundel G; Krikler R
    Clin Genet; 1975 Mar; 7(3):192-6. PubMed ID: 1139788
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformations.
    Mertens F; Johansson B; Forslund M; Olsson M; Kristoffersson U
    Clin Genet; 1987 Jul; 32(1):46-8. PubMed ID: 3621653
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome.
    Magnelli NC; Therman E
    J Med Genet; 1975 Mar; 12(1):105-8. PubMed ID: 1121016
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The phenotype of ring chromosome 3.
    Wilson GN; Pooley J; Parker J
    J Med Genet; 1982 Dec; 19(6):471-3. PubMed ID: 7154048
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Partial trisomy 15 in a young girl.
    Mankinen CB; Hold JG; Sears JW
    Clin Genet; 1976 Jul; 10(1):27-32. PubMed ID: 949862
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Rethoré MO; Hoehn H; Rott HD; Couturier J; Dutrillaux B; Lejeune J
    Humangenetik; 1973 Apr; 18(2):129-38. PubMed ID: 4124236
    [No Abstract]   [Full Text] [Related]  

  • 29. A long unidentifiable extra chromosomal segment--a possible duplication of human 7q.
    Wahrman J; Cohen MM; Rosenmann A; Goitein R; Richler C; Dagan J
    Cytogenet Cell Genet; 1978; 20(1-6):160-8. PubMed ID: 648175
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cytogenetics of 50 patients with mental retardation and multiple congenital anomalies and 50 normal subjects. Madison blind study IV.
    Magnelli NC
    Clin Genet; 1976 Feb; 9(2):169-82. PubMed ID: 1248176
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ring chromosome 14 in a mentally retarded girl.
    Iselius L; Ritzén M; Bui TH; Olsson K; Eklöf O
    Acta Paediatr Scand; 1980 Nov; 69(6):803-6. PubMed ID: 7211367
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital hepatic fibrosis, cystic kidneys, mental retardation, and facial dysmorphy: a new report of an autosomal recessive syndrome.
    Labrune P; Lange JC; Bedossa P; Chaussain JL; Odievre M
    J Pediatr Gastroenterol Nutr; 1990 May; 10(4):540-3. PubMed ID: 2193138
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH; Broske SP; Moore CM; Thomas GH; Neill CA
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
    [TBL] [Abstract][Full Text] [Related]  

  • 34. De novo direct tandem duplication of the proximal long arm of chromosome 2: 46,XX,dir dup(2)(q11 X 2q14 X 2).
    Mu Y; Van Dyke DL; Weiss L; Olgac S
    J Med Genet; 1984 Feb; 21(1):57-8. PubMed ID: 6694186
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Bisatellited dicentric chromosome: a report on a case with karyotype 47,XY, + psu dic(22)t(22;22)(22pter to cen to 22q11::22q11 to 22pter).
    Weilong G; Aide Y; Hongbao F; Shumou L; Ju Y
    Hum Genet; 1982; 61(4):325-8. PubMed ID: 7152517
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Multiple "marker" chromosomes: a novel cytogenetic finding in a patient with mental retardation and congenital anomalies.
    Tozzi C; Calvieri F; Alesi L; Neri G
    Am J Med Genet; 1988 Feb; 29(2):355-9. PubMed ID: 3354606
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Structural anomaly (inv (p-q+)?) of a C + X group chromosome in a dysplastic boy with dissociated mental development].
    Keutel J; Schubert W
    Humangenetik; 1969; 7(2):119-25. PubMed ID: 5799490
    [No Abstract]   [Full Text] [Related]  

  • 38. A cytogenetic study of children with clinically unclassifiable multiple congenital malformations and mental retardation.
    Narahara K
    Acta Med Okayama; 1981 Nov; 35(5):343-55. PubMed ID: 6458997
    [TBL] [Abstract][Full Text] [Related]  

  • 39. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.
    Koç A; Kan D; Karaer K; Ergün MA; Karaoğuz MY; Gücüyener K; Hinreiner S; Liehr T; Perçin EF
    Eur J Pediatr; 2008 Jun; 167(6):655-9. PubMed ID: 17668239
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
    Stoll C; Levy J; Roth MP
    J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.