BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 3377005)

  • 1. A new autosomal recessive lethal chondrodystrophy with congenital hydrops.
    Greenberg CR; Rimoin DL; Gruber HE; DeSa DJ; Reed M; Lachman RS
    Am J Med Genet; 1988 Mar; 29(3):623-32. PubMed ID: 3377005
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder.
    Chitayat D; Gruber H; Mullen BJ; Pauzner D; Costa T; Lachman R; Rimoin DL
    Am J Med Genet; 1993 Aug; 47(2):272-7. PubMed ID: 8213919
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Autosomal recessive omodysplasia.
    Stoll C; Pennerath A; Poirat P
    Ann Genet; 1995; 38(2):97-101. PubMed ID: 7486832
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Greenberg dysplasia (hydrops-ectopic calcification-moth-eaten skeletal dysplasia): prenatal ultrasound diagnosis and review of literature.
    Trajkovski Z; Vrcakovski M; Saveski J; Gucev ZS
    Am J Med Genet; 2002 Sep; 111(4):415-9. PubMed ID: 12210303
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new category of lethal short-limbed dwarfism.
    Knowles S; Winter R; Rimoin D
    Am J Med Genet; 1986 Sep; 25(1):41-6. PubMed ID: 3799722
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
    Franceschini P; Testa A; Bogetti G; Girardo E; Guala A; Lopez-Bell G; Buzio G; Ferrario E; Piccato E
    Am J Med Genet; 1992 Jan; 42(1):112-6. PubMed ID: 1308349
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new lethal autosomal recessive skeletal dysplasia with associated dysmorphic features.
    Morton JE; Kilby MD; Rushton I
    Clin Dysmorphol; 1998 Apr; 7(2):109-14. PubMed ID: 9571280
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneity.
    Aleck KA; Grix A; Clericuzio C; Kaplan P; Adomian GE; Lachman R; Rimoin DL
    Am J Med Genet; 1987 Jun; 27(2):295-312. PubMed ID: 3605216
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A distinct lethal neonatal chondrodysplasia with snail-like pelvis: Schneckenbecken dysplasia.
    Borochowitz Z; Jones KL; Silbey R; Adomian G; Lachman R; Rimoin DL
    Am J Med Genet; 1986 Sep; 25(1):47-59. PubMed ID: 3799723
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Skeletal dysplasias with gracile bones: three new cases, including two offspring of a mother with a dwarfing condition.
    Costa T; Azouz EM; Fitzpatrick J; Kamel-Reid S; Smith CR; Silver MM
    Am J Med Genet; 1998 Mar; 76(2):125-32. PubMed ID: 9511974
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spondyloepimetaphyseal dysplasia (SEMD) Shohat type.
    Figuera LE; Ramírez-Dueñas ML; Gallegos-Arreola MP; Cantú JM
    Am J Med Genet; 1994 Jul; 51(3):213-5. PubMed ID: 8074146
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
    Janssen HC; Schaap C; Vandevijver N; Moerman P; de Die-Smulders CE; Fryns JP
    J Med Genet; 1999 Jun; 36(6):481-4. PubMed ID: 10874639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lethal neonatal chondrodysplasias in the West of Scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, Glasgow variant.
    Connor JM; Connor RA; Sweet EM; Gibson AA; Patrick WJ; McNay MB; Redford DH
    Am J Med Genet; 1985 Oct; 22(2):243-53. PubMed ID: 3901754
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
    Miny P; Lenz W
    Am J Med Genet; 1985 Jun; 21(2):317-24. PubMed ID: 4014313
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial Blomstrand chondrodysplasia with advanced skeletal maturation: further delineation.
    Loshkajian A; Roume J; Stanescu V; Delezoide AL; Stampf F; Maroteaux P
    Am J Med Genet; 1997 Aug; 71(3):283-8. PubMed ID: 9268097
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Prenatal sonographic diagnosis of a case of Desbuquois familial osseous dysplasia].
    Grischke EM; Tröger J; Schroeder-Kurth T; Schmidt W
    Z Geburtshilfe Perinatol; 1989; 193(4):195-7. PubMed ID: 2678787
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.
    Opitz JM; Spranger JW; Stöss HR; Pesch HJ; Azadeh B
    Am J Med Genet; 1987 Mar; 26(3):583-90. PubMed ID: 3565474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fibrochondrogenesis.
    Kulkarni ML; Matadh PS; Praveen Prabhu SP; Kulkarni PM
    Indian J Pediatr; 2005 Apr; 72(4):355-7. PubMed ID: 15876767
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Schneckenbecken dysplasia in fetus: report of four cases.
    Lahmar-Boufaroua A; Yacoubi MT; Belaid L; Delezoide AL
    Fetal Diagn Ther; 2009; 25(2):216-9. PubMed ID: 19407457
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.