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 *

117 related articles for article (PubMed ID: 879167)

  • 1. Consanguinity analysis in Israeli mental retardates.
    Costeff H; Cohen BE; Weller L; Rahman D
    Am J Hum Genet; 1977 Jul; 29(4):339-49. PubMed ID: 879167
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Relative importance of genetic and nongenetic etiologies in idiopathic mental retardation: estimates based on analysis of medical histories.
    Costeff H; Cohen BE; Weller L
    Ann Hum Genet; 1983 Jan; 47(1):83-93. PubMed ID: 6838171
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parental consanguinity among Israeli mental retardates.
    Costeff H; Cohen BE; Weller L
    Acta Paediatr Scand; 1972 Jul; 61(4):452-8. PubMed ID: 5041393
    [No Abstract]   [Full Text] [Related]  

  • 4. Consanguinity analysis of congenital deafness in Northern Israel.
    Costeff H; Dar H
    Am J Hum Genet; 1980 Jan; 32(1):64-8. PubMed ID: 7361765
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pathogenic factors in idiopathic mental retardation.
    Costeff H; Cohen BE; Weller L; Kleckner H
    Dev Med Child Neurol; 1981 Aug; 23(4):484-93. PubMed ID: 7196853
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Consanguinity analysis in heterogeneous populations.
    Costeff H
    Am J Hum Genet; 1977 Jul; 29(4):329-38. PubMed ID: 879166
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial mental retardation: a continuing dilemma.
    Zigler E
    Science; 1967 Jan; 155(3760):292-8. PubMed ID: 5333962
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic epidemiology of an institutionalized cohort of mental retardates.
    Morton NE; Matsuura J; Bart R; Lew R
    Clin Genet; 1978 Jun; 13(6):449-61. PubMed ID: 668181
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families.
    Ahmed I; Rafiq MA; Vincent JB; Bhatti A; Ayub M; John P
    Acta Neuropsychiatr; 2015 Feb; 27(1):38-47. PubMed ID: 25434728
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Effect of inbreeding on IQ and mental retardation.
    Morton NE
    Proc Natl Acad Sci U S A; 1978 Aug; 75(8):3906-8. PubMed ID: 279005
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Consanguinity, intracommunity and intercommunity marriages in a population sample of Israeli Jews.
    Cohen T; Vardi-Saliternik R; Friedlander Y
    Ann Hum Biol; 2004; 31(1):38-48. PubMed ID: 14742164
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.
    Najmabadi H; Motazacker MM; Garshasbi M; Kahrizi K; Tzschach A; Chen W; Behjati F; Hadavi V; Nieh SE; Abedini SS; Vazifehmand R; Firouzabadi SG; Jamali P; Falah M; Seifati SM; Grüters A; Lenzner S; Jensen LR; Rüschendorf F; Kuss AW; Ropers HH
    Hum Genet; 2007 Mar; 121(1):43-8. PubMed ID: 17120046
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Amino acid disorders in mental retardation: a two-decade study from Andhra Pradesh.
    Swarna M; Jyothy A; Usha Rani P; Reddy PP
    Biochem Genet; 2004 Apr; 42(3-4):85-98. PubMed ID: 15168722
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial hydrocephalus of prenatal onset.
    Zlotogora J; Sagi M; Cohen T
    Am J Med Genet; 1994 Jan; 49(2):202-4. PubMed ID: 8116668
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The hyperphenylalaninemias in Israel.
    Cohen BE; Szeinberg A; Pollak S; Peled I; Likverman S; Crispin M
    Isr J Med Sci; 1973; 9(9):1393-5. PubMed ID: 4775121
    [No Abstract]   [Full Text] [Related]  

  • 16. Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups.
    Stoffman N; Magal N; Shohat T; Lotan R; Koman S; Oron A; Danon Y; Halpern GJ; Lifshitz Y; Shohat M
    Eur J Hum Genet; 2000 Apr; 8(4):307-10. PubMed ID: 10854115
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial hydroxykynureninuria.
    Reddi OS; Reddy MV; Reddy KR
    Hum Hered; 1978; 28(3):238-40. PubMed ID: 649181
    [No Abstract]   [Full Text] [Related]  

  • 18. Estimated number of loci for autosomal recessive severe nerve deafness within the Israeli Jewish population, with implications for genetic counseling.
    Brownstein Z; Friedlander Y; Peritz E; Cohen T
    Am J Med Genet; 1991 Dec; 41(3):306-12. PubMed ID: 1789284
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial dwarfism with high IR-GH: report of two affected sibs with genetic and epidemiologic considerations.
    Saldanha PH; Toledo SP
    Hum Genet; 1981; 59(4):367-72. PubMed ID: 7333592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.
    Basel-Vanagaite L; Alkelai A; Straussberg R; Magal N; Inbar D; Mahajna M; Shohat M
    J Med Genet; 2003 Oct; 40(10):729-32. PubMed ID: 14569116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.