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 *

127 related articles for article (PubMed ID: 15365460)

  • 21. The pattern of skeletal anomalies in the cervical spine, hands and feet in patients with Saethre-Chotzen syndrome and Muenke-type mutation.
    Trusen A; Beissert M; Collmann H; Darge K
    Pediatr Radiol; 2003 Mar; 33(3):168-72. PubMed ID: 12612814
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The Catel-Manzke syndrome in a female infant.
    Kant SG; Oudshoorn A; Gi CV; Zonderland HM; Van Haeringen A
    Genet Couns; 1998; 9(3):187-90. PubMed ID: 9777339
    [TBL] [Abstract][Full Text] [Related]  

  • 23. F-syndrome (F-form of acro-pectoro-vertebral dysplasia): report on a second family.
    Camera G; Camera A; Pozzolo S; Costa M; Mantero R
    Am J Med Genet; 1995 Jul; 57(3):472-5. PubMed ID: 7677153
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [A rare case of multiple sesamoid bones in the hands and feet].
    Borsoni GO
    Radiol Med; 1990 Apr; 79(4):388-90. PubMed ID: 2377758
    [No Abstract]   [Full Text] [Related]  

  • 25. Cenani-Lenz syndrome: report of a new case and review of the literature.
    Nezarati MM; McLeod DR
    Clin Dysmorphol; 2002 Jul; 11(3):215-8. PubMed ID: 12072805
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cooks syndrome: a case report and brief review.
    Brennan CB; Buehler T; Lesher JL
    Pediatr Dermatol; 2013; 30(4):e52-3. PubMed ID: 22329539
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cystic hygroma and hirsutism in a child with Catel-Manzke syndrome.
    Kapoor S; Ghosh V; Dhua A; Aggarwal SK
    Clin Dysmorphol; 2011 Apr; 20(2):117-120. PubMed ID: 21383555
    [No Abstract]   [Full Text] [Related]  

  • 28. Pierre Robin sequence and hyperphalangy--a genetic entity (Catel-Manzke syndrome).
    Brude E
    Eur J Pediatr; 1984 Aug; 142(3):222-3. PubMed ID: 6540680
    [TBL] [Abstract][Full Text] [Related]  

  • 29. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.
    Lin HJ; Kakkis ED; Eteson DJ; Lachman RS
    Am J Med Genet; 1993 Sep; 47(4):534-9. PubMed ID: 8256819
    [TBL] [Abstract][Full Text] [Related]  

  • 30. RSH (Smith-Lemli-Opitz) syndrome: "severe" phenotype with ectrodactyly.
    de Jong G; Kirby PA; Muller LM
    Am J Med Genet; 1998 Jan; 75(3):283-7. PubMed ID: 9475598
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Otospondylomegaepiphyseal dysplasia: report of three sibs and review of the literature.
    al Gazali LI; Lytle W
    Clin Dysmorphol; 1994 Jan; 3(1):46-54. PubMed ID: 8205326
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mirror hands and feet: a further case of Laurin-Sandrow syndrome.
    Hatchwell E; Dennis N
    J Med Genet; 1996 May; 33(5):426-8. PubMed ID: 8733058
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.
    Nevin NC; Thomas PS; Eedy DJ; Shepherd C
    J Med Genet; 1995 Aug; 32(8):638-41. PubMed ID: 7473658
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Two isolated cases with symmetrically absent hands and feet.
    Horn D; Kolb GP
    Clin Dysmorphol; 1994 Jul; 3(3):228-33. PubMed ID: 7981858
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A; Donnai D
    Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism.
    Ehmke N; Cusmano-Ozog K; Koenig R; Holtgrewe M; Nur B; Mihci E; Babcock H; Gonzaga-Jauregui C; Overton JD; Xiao J; Martinez AF; Muenke M; Balzer A; Jochim J; El Choubassi N; Fischer-Zirnsak B; Huber C; Kornak U; Elsea SH; Cormier-Daire V; Ferreira CR
    Bone; 2020 Apr; 133():115219. PubMed ID: 31923704
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Abnormalities of the hands and feet in the fetus: sonographic findings.
    Bromley B; Benacerraf B
    AJR Am J Roentgenol; 1995 Nov; 165(5):1239-43. PubMed ID: 7572511
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [A case of congenital hypodactyly of the hand and foot].
    Mamedov AG; Seidov MM
    Ortop Travmatol Protez; 1991 Apr; (4):51-2. PubMed ID: 1754179
    [No Abstract]   [Full Text] [Related]  

  • 39. A novel patient with Cooks syndrome supports splitting from "classic" brachydactyly type B.
    Castori M; Brancati F; Mingarelli R; Mundlos S; Dallapiccola B
    Am J Med Genet A; 2007 Jan; 143A(2):195-9. PubMed ID: 17163524
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Craniosynostosis with Marfan syndrome, hand and foot anomalies.
    Shah AM; Chattopadhyay A; Kher A; Bharucha BA; Karapurkar AP
    Clin Dysmorphol; 1996 Jul; 5(3):263-6. PubMed ID: 8818457
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.