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 *

170 related articles for article (PubMed ID: 8488837)

  • 1. Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation.
    Crosby JL; Varnum DS; Nadeau JH
    Am J Hum Genet; 1993 May; 52(5):866-74. PubMed ID: 8488837
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Human malformations similar to those in the mouse mutation disorganization (Ds).
    Robin NH; Adewale OO; McDonald-McGinn D; Nadeau JH; Zackai EH; Bućan M
    Hum Genet; 1993 Nov; 92(5):461-4. PubMed ID: 8244336
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Disorganization in mice and humans and its relation to sporadic birth defects.
    Robin NH; Abbadi N; McCandless SE; Nadeau JH
    Am J Med Genet; 1997 Dec; 73(4):425-36. PubMed ID: 9415470
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disorganization is a completely dominant gain-of-function mouse mutation causing sporadic developmental defects.
    Crosby JL; Varnum DS; Washburn LL; Nadeau JH
    Mech Dev; 1992 May; 37(3):121-6. PubMed ID: 1498039
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Disorganization in mice and humans.
    Robin NH; Nadeau JH
    Am J Med Genet; 2001 Jul; 101(4):334-8. PubMed ID: 11471156
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital anal anomalies in two families with the Opitz G syndrome.
    Tolmie JL; Coutts N; Drainer IK
    J Med Genet; 1987 Nov; 24(11):688-91. PubMed ID: 3430544
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Role of the Nh (Non-hair) mutation in the development of dermatitis and hyperproduction of IgE in DS-Nh mice.
    Watanabe A; Takeuchi M; Nagata M; Nakamura K; Nakao H; Yamashita H; Makino S; Harada M; Hirasawa T
    Exp Anim; 2003 Oct; 52(5):419-23. PubMed ID: 14625409
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two additional patients representing the possible human homologue for the mouse mutant disorganisation (Ds).
    Lin AE
    J Med Genet; 1991 Sep; 28(9):645-7. PubMed ID: 1956071
    [No Abstract]   [Full Text] [Related]  

  • 9. Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome.
    Yan J; Keener VW; Bi W; Walz K; Bradley A; Justice MJ; Lupski JR
    Hum Mol Genet; 2004 Nov; 13(21):2613-24. PubMed ID: 15459175
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiple anomalies possibly caused by a human homologue to the mouse disorganization (Ds) gene.
    de Michelena MI; Stachurska A
    Clin Dysmorphol; 1993 Apr; 2(2):131-4. PubMed ID: 8281274
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation.
    Summitt RL; Tharapel AT; Wilroy RS
    Eur J Pediatr; 1977 Jul; 125(3):169-74. PubMed ID: 885143
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Developmental anomalies in monozygous twins resembling the human homologue of the mouse mutant disorganization.
    Wainwright H; Viljoen D
    Clin Dysmorphol; 1993 Apr; 2(2):135-9. PubMed ID: 8281275
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mortality and pathological findings in C (Opitz trigonocephaly) syndrome.
    Opitz JM; Putnam AR; Comstock JM; Chin S; Byrne JL; Kennedy A; Frikke MJ; Bernard C; Albrecht S; Der Kaloustian V; Szakacs JG
    Fetal Pediatr Pathol; 2006; 25(4):211-31. PubMed ID: 17162528
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal dominant inheritance of Weaver syndrome.
    Fryer A; Smith C; Rosenbloom L; Cole T
    J Med Genet; 1997 May; 34(5):418-9. PubMed ID: 9152841
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pericentric inversion of chromosome "20" associated with congenital anomalies.
    Valvova G; Demirev G
    Folia Med (Plovdiv); 1980; 22(4):44-6. PubMed ID: 6790380
    [No Abstract]   [Full Text] [Related]  

  • 16. Break points on 18 ring chromosome of a girl with congenital anomalies.
    Muramoto J; Honda J; Niitsuma K; Fukushima T
    Fukushima J Med Sci; 1978; 25(3-4):131-4. PubMed ID: 756386
    [No Abstract]   [Full Text] [Related]  

  • 17. Animal model: skeletal anomalies in mice with cleidocranial dysplasia.
    Sillence DO; Ritchie HE; Selby PB
    Am J Med Genet; 1987 May; 27(1):75-85. PubMed ID: 3605208
    [TBL] [Abstract][Full Text] [Related]  

  • 18. "Disorganization" gene in mutations.
    Winter RM; Donnai D
    Am J Med Genet; 1990 Nov; 37(3):435-6. PubMed ID: 2260581
    [No Abstract]   [Full Text] [Related]  

  • 19. Vertical transmission of the Ohdo blepharophimosis syndrome.
    Mhanni AA; Dawson AJ; Chudley AE
    Am J Med Genet; 1998 May; 77(2):144-8. PubMed ID: 9605288
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetic aspects of teratology].
    Laziuk GI; Lur'e IV
    Vestn Akad Med Nauk SSSR; 1982; (6):24-32. PubMed ID: 7051613
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.