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 *

220 related articles for article (PubMed ID: 3857858)

  • 1. Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorder.
    Seemanová E; Passarge E; Beneskova D; Houstĕk J; Kasal P; Sevcíková M
    Am J Med Genet; 1985 Apr; 20(4):639-48. PubMed ID: 3857858
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive nonsyndromal microcephaly with normal intelligence.
    Teebi AS; Al-Awadi SA; White AG
    Am J Med Genet; 1987 Feb; 26(2):355-9. PubMed ID: 3812587
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS; Kaurah P
    Am J Med Genet; 1996 Dec; 66(3):257-60. PubMed ID: 8985482
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.
    Seeman P; Gebertová K; Paderová K; Sperling K; Seemanová E
    Pediatr Neurol; 2004 Mar; 30(3):195-200. PubMed ID: 15033202
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A familial aggregate of common variable immunodeficiency, Hodgkin disease and other malignancies in Newfoundland--II. Genealogical analysis and conclusions regarding hereditary determinants.
    Salmon D; Landre MF; Fraser GR; Buehler SK; Crumley J; Marshall WH
    Clin Invest Med; 1979; 2(4):175-81. PubMed ID: 583572
    [No Abstract]   [Full Text] [Related]  

  • 6. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?
    Kotzot D; Richter K; Gierth-Fiebig K
    Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An apparently new syndrome of microcephalic primordial dwarfism and cataracts.
    Toriello HV; Horton WA; Oostendorp A; Waterman DF; Higgins JV
    Am J Med Genet; 1986 Sep; 25(1):1-8. PubMed ID: 3799711
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A familial aggregate of common variable immunodeficiency, Hodgkin disease and other malignancies in Newfoundland--I. Clinical features.
    Marshall WH; Buehler SK; Crumley J; Salmon D; Landre MF; Fraser GR
    Clin Invest Med; 1979; 2(4):153-9. PubMed ID: 583571
    [No Abstract]   [Full Text] [Related]  

  • 9. A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parents.
    Stoll C; Alembik Y; Lutz P
    Genet Couns; 1994; 5(2):161-5. PubMed ID: 7917125
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal recessive microcephaly with severe psychomotor retardation.
    Scheffer IE; Baraitser M; Wilson J; Godfrey C; Brett EM
    Neuropediatrics; 1992 Feb; 23(1):53-6. PubMed ID: 1565220
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome.
    Chrzanowska KH; Kleijer WJ; Krajewska-Walasek M; Białecka M; Gutkowska A; Goryluk-Kozakiewicz B; Michałkiewicz J; Stachowski J; Gregorek H; Lysón-Wojciechowska G
    Am J Med Genet; 1995 Jul; 57(3):462-71. PubMed ID: 7545870
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected child.
    Tolmie JL; McNay M; Stephenson JB; Doyle D; Connor JM
    Am J Med Genet; 1987 Jul; 27(3):583-94. PubMed ID: 3307411
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks.
    Digweed M; Sperling K
    DNA Repair (Amst); 2004; 3(8-9):1207-17. PubMed ID: 15279809
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Microcephaly with chromosomal instability and immunodeficiency--Nijmegen syndrome].
    Chrzanowska KH
    Pediatr Pol; 1996 Mar; 71(3):223-34. PubMed ID: 8966094
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Neonatal diabetes mellitus and microcephaly. Indications for autosomal recessive inheritance].
    Reus S; Egidi R; Otten A; Aulepp U
    Monatsschr Kinderheilkd; 1992 Nov; 140(11):803-7. PubMed ID: 1470185
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family.
    Moreno LA; Gottrand F; Turck D; Manouvrier-Hanu S; Mazingue F; Morisot C; Le Deist F; Ricour C; Nihoul-Feketé C; Debeugny P
    Am J Med Genet; 1990 Sep; 37(1):143-6. PubMed ID: 2240032
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
    Børglum AD; Balslev T; Haagerup A; Birkebaek N; Binderup H; Kruse TA; Hertz JM
    Eur J Hum Genet; 2001 Oct; 9(10):753-7. PubMed ID: 11781686
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal recessive microcephaly and micromelia in Cree Indians.
    Ives EJ; Houston CS
    Am J Med Genet; 1980; 7(3):351-60. PubMed ID: 7468660
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16.
    Chandler KE; Del Rio A; Rakshi K; Springell K; Williams DK; Stoodley N; Woods CG; Pilz DT
    Brain; 2006 Jan; 129(Pt 1):272-7. PubMed ID: 16272165
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetic analysis of microcephaly].
    Danielov MB
    Genetika; 1976; 12(8):151-6. PubMed ID: 137165
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.