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 *

103 related articles for article (PubMed ID: 6509163)

  • 1. Craniofacial development in arthrogryposis (congenital contractures).
    Hall JG
    Birth Defects Orig Artic Ser; 1984; 20(3):99-111. PubMed ID: 6509163
    [No Abstract]   [Full Text] [Related]  

  • 2. Part II. Amyoplasia: twinning in amyoplasia--a specific type of arthrogryposis with an apparent excess of discordantly affected identical twins.
    Hall JG; Reed SD; McGillivray BC; Herrmann J; Partington MW; Schinzel A; Shapiro J; Weaver DD
    Am J Med Genet; 1983 Aug; 15(4):591-9. PubMed ID: 6684397
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Arthrogryposis associated with unsuccessful attempts at termination of pregnancy.
    Hall JG
    Am J Med Genet; 1996 May; 63(1):293-300. PubMed ID: 8723123
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Importance of growth for evaluation of craniofacial morphology in identical twins].
    Velísková E
    Cesk Stomatol; 1977 Jul; 77(4):271-6. PubMed ID: 269021
    [No Abstract]   [Full Text] [Related]  

  • 5. Prevalence of multiple congenital contractures including arthrogryposis multiplex congenita in Alberta, Canada, and a strategy for classification and coding.
    Lowry RB; Sibbald B; Bedard T; Hall JG
    Birth Defects Res A Clin Mol Teratol; 2010 Dec; 88(12):1057-61. PubMed ID: 21157886
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transient neonatal arthrogryposis: a presumed sequel of antenatal hypoxia.
    Robinow M
    Am J Med Genet; 1986 Sep; 25(1):167-8. PubMed ID: 3799717
    [No Abstract]   [Full Text] [Related]  

  • 7. [Pair comparison of the jaw development in monozygotic twins].
    Klink-Heckmann U; Dahl T
    Zahn Mund Kieferheilkd Zentralbl; 1977; 65(7):762-9. PubMed ID: 146367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [The sequence of fetal akinesia/hypokinesia, Pena-Shokeir syndrome, multiple congenital arthrogryposis and/or short umbilical cord: conceptual delimitation].
    Gonzalez de Dios J; García-Alix A
    An Esp Pediatr; 1998 Feb; 48(2):197-200. PubMed ID: 9577032
    [No Abstract]   [Full Text] [Related]  

  • 9. Differences in protocols of craniofacial development related to twinship and zygosity.
    Boklage CE
    J Craniofac Genet Dev Biol; 1984; 4(2):151-69. PubMed ID: 6540276
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fetal arthrogryposis and maternal serum antibodies.
    Dalton P; Clover L; Wallerstein R; Stewart H; Genzel-Boroviczeny O; Dean A; Vincent A
    Neuromuscul Disord; 2006 Aug; 16(8):481-91. PubMed ID: 16919948
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Part I. Amyoplasia: a common, sporadic condition with congenital contractures.
    Hall JG; Reed SD; Driscoll EP
    Am J Med Genet; 1983 Aug; 15(4):571-90. PubMed ID: 6614047
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatally diagnosed Arthrogryposis multiplex congenita due to pathological changes in the fetal heart rate pattern.
    Leeners B; Sauer AI; Rath W; Funk A
    Prenat Diagn; 2005 Jul; 25(7):625-6. PubMed ID: 16034831
    [No Abstract]   [Full Text] [Related]  

  • 13. [Lethal nemalinic myopathy and congenital arthrogryposis or fetal hypokinesia sequence?].
    González de Dios J
    Rev Neurol; 2002 Jun 16-30; 34(12):1197-8. PubMed ID: 12134290
    [No Abstract]   [Full Text] [Related]  

  • 14. [Arthrogryposis in childhood. Arthrogryposis multiplex congenita].
    Pous JG
    Chir Pediatr; 1981; 22(5):289-363. PubMed ID: 7285264
    [No Abstract]   [Full Text] [Related]  

  • 15. [Hip in arthrogryposis multiplex congenita].
    Södergard J
    Rev Chir Orthop Reparatrice Appar Mot; 1996; 82(5):403-9. PubMed ID: 8991163
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Congenital taxoplasmosis in twins in own material].
    Lipka B; Milewska-Bobula B; Dunin-Wasowicz D; Kassur-Siemieńska B; Idzik M; Szreter M; Witkowska-Vogtt E
    Wiad Parazytol; 2004; 50(2):187-91. PubMed ID: 16859024
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Long first metacarpal in monozygotic twins with probable Baller-Gerold syndrome.
    Franceschini P; Licata D; Guala A; Di Cara G; Signorile F; Franceschini D; Genitori L; Restagno G
    Am J Med Genet; 1998 Dec; 80(4):303-8. PubMed ID: 9856554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Embryonic myosin heavy-chain mutations cause distal arthrogryposis and developmental myosin myopathy that persists postnatally.
    Tajsharghi H; Kimber E; Kroksmark AK; Jerre R; Tulinius M; Oldfors A
    Arch Neurol; 2008 Aug; 65(8):1083-90. PubMed ID: 18695058
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Arthrogryposis.
    Hall JG
    Am Fam Physician; 1989 Jan; 39(1):113-9. PubMed ID: 2643273
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Discordant congenital malformations in monozygous twins: the amniotic band disruption complex.
    Pysher TJ
    Diagn Gynecol Obstet; 1980; 2(3):221-5. PubMed ID: 7439020
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.