BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 9375925)

  • 1. Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family.
    Mégarbané A; Tomey K; Wakim G
    Am J Med Genet; 1997 Nov; 73(1):67-71. PubMed ID: 9375925
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report.
    Hamel BC; Draaisma JM; Pinckers AJ; Boetes C; Hoppe RL; Ropers HH; Brunner HG
    Am J Med Genet; 1995 Apr; 56(3):312-6. PubMed ID: 7778598
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.
    Richieri-Costa A; Guion-Almeida ML; Pagnan NA
    Am J Med Genet; 1992 Dec; 44(6):800-2. PubMed ID: 1481850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frank-ter Haar syndrome with unusual clinical features.
    Dundar M; Saatci C; Tasdemir S; Akcakus M; Caglayan AO; Ozkul Y
    Eur J Med Genet; 2009; 52(4):247-9. PubMed ID: 19303467
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frank-Ter Haar Syndrome.
    Saeed M; Shair QA; Saleem SM
    J Coll Physicians Surg Pak; 2011 Apr; 21(4):252-3. PubMed ID: 21453629
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Microcephaly with large anterior fontanelle, generalized convulsions, micropenis, and distinct anomalies of the hands and feet. Another example of Wiedemann syndrome?
    Nevin NC; Stewart FJ; Corkey CW; Bell BA
    Clin Genet; 1994 Aug; 46(2):205-8. PubMed ID: 7529662
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A distinct skeletal dysplasia in an infant from consanguineous parents.
    Cantú JM; Manzano C; Pagán P; García-Cruz D; Hernández A
    Birth Defects Orig Artic Ser; 1977; 13(3B):139-47. PubMed ID: 890089
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Feingold syndrome: report of a new family and review.
    Courtens W; Levi S; Verbelen F; Verloes A; Vamos E
    Am J Med Genet; 1997 Nov; 73(1):55-60. PubMed ID: 9375923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Vertebral anomalies in a new family with ODED syndrome.
    Piersall LD; Dowton SB; McAlister WH; Waggoner DJ
    Clin Genet; 2000 Jun; 57(6):444-8. PubMed ID: 10905665
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Post-natal short stature, short limbs, brachydactyly, facial abnormalities, and delayed bone age: a new syndrome?
    Mégarbané A; Rassi S; Estephan F; Kouba-Hreich E
    Am J Med Genet A; 2004 Feb; 125A(1):57-60. PubMed ID: 14755467
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousins.
    Dundar M; Demiryilmaz F; Demiryilmaz I; Kumandas S; Erkilic K; Kendirci M; Tuncel M; Ozyazgan I; Tolmie JL
    Clin Genet; 1997 Jan; 51(1):61-4. PubMed ID: 9084938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sandrow syndrome of mirror hands and feet and facial abnormalities.
    Kogekar N; Teebi AS; Vockley J
    Am J Med Genet; 1993 Apr; 46(2):126-8. PubMed ID: 8387243
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literature.
    Ausems MG; Ippel PF; Renardel de Lavalette PA
    Clin Dysmorphol; 1994 Jan; 3(1):21-30. PubMed ID: 8205322
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.
    Borochowitz Z; Langer LO; Gruber HE; Lachman R; Katznelson MB; Rimoin DL
    Am J Med Genet; 1993 Feb; 45(3):320-6. PubMed ID: 8434618
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mild facial dysmorphism and quasidominant inheritance in Cenani-Lenz syndrome.
    Temtamy SA; Ismail S; Nemat A
    Clin Dysmorphol; 2003 Apr; 12(2):77-83. PubMed ID: 12868467
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A distinct autosomal recessive disorder of limb development with preaxial brachydactyly, phalangeal duplication, symphalangism and hyperphalangism.
    Race H; Hall CM; Harrison MG; Quarrell OW; Wakeling EL
    Clin Dysmorphol; 2010 Jan; 19(1):23-27. PubMed ID: 19952732
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
    Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New syndrome of macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay.
    Bagatelle R; Cassidy SB
    Am J Med Genet; 1995 Jan; 55(3):367-71. PubMed ID: 7537019
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new acro-cranio-facial dysostosis syndrome in sisters.
    Kaplan P; Plauchu H; Fitch N; Jéquier S
    Am J Med Genet; 1988 Jan; 29(1):95-106. PubMed ID: 3344780
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Associated malformations of the head and extremities].
    Tridon P
    J Genet Hum; 1974 Dec; 22(4):365-80. PubMed ID: 4282383
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.