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 *

142 related articles for article (PubMed ID: 7735504)

  • 21. Mesomelic shortening of the upper extremities with spur formation and cutaneous dimpling.
    Kerner B; Rimoin DL; Lachman RS
    Pediatr Radiol; 1998 Oct; 28(10):794-7. PubMed ID: 9799303
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Oral-facial-digital syndrome type 1 is another dominant polycystic kidney disease: clinical, radiological and histopathological features of a new kindred.
    Feather SA; Winyard PJ; Dodd S; Woolf AS
    Nephrol Dial Transplant; 1997 Jul; 12(7):1354-61. PubMed ID: 9249769
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Craniocarpotarsal dysplasia: the whistling face syndrome.
    Guyuron B; Winkler PA
    Ann Plast Surg; 1988 Jan; 20(1):86-8. PubMed ID: 3341720
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A new syndrome of microtia with mixed type hearing loss, renal agenesis, and multiple skeletal anomalies.
    Demir Y; Samli H; Yucel A; Yilmaz MD; Haktanir NT; Maralcan G; Solak M
    Am J Med Genet A; 2006 Apr; 140(7):747-51. PubMed ID: 16502432
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Potter's syndrome: bilateral renal agenesis (a report of two cases emphasizing associated malformations).
    Tinaztepe K; Balci S; Tinaztepe B; Dağli E
    Turk J Pediatr; 1983; 25(3):179-87. PubMed ID: 6673215
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. [Congenital eyelid ptosis and dental anomalies in the Francheschetti syndrome].
    Crăiţoiu M; Preoteasa D
    Oftalmologia; 1994; 38(2):135-7, 140. PubMed ID: 8186207
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Unilateral Potter syndrome with amelia.
    Barta L; Balogh L; Szinay G; Regöly-Mérei A
    Acta Paediatr Acad Sci Hung; 1981; 22(3):195-9. PubMed ID: 7304159
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Potter's syndrome with mental retardation (auro-renal syndrome; reno-facial dysplasia).
    Jancar J
    J Ment Defic Res; 1969 Mar; 13(1):8-12. PubMed ID: 5779632
    [No Abstract]   [Full Text] [Related]  

  • 30. Lacrimo-auriculo-dento-digital syndrome: evidence for lower limb involvement and severe congenital renal anomalies.
    Bamforth JS; Kaurah P
    Am J Med Genet; 1992 Aug; 43(6):932-7. PubMed ID: 1415342
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Microcephalic osteodysplastic dysplasia.
    Hersh JH; Joyce MR; Spranger J; Goatley EC; Lachman RS; Bhatt S; Rimoin DL
    Am J Med Genet; 1994 Jul; 51(3):194-9. PubMed ID: 8074143
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
    Meinecke P
    Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Limb/pelvis-hypoplasia/aplasia syndrome--further delineation of phenotype.
    Gupta N; Kabra M
    Fetal Pediatr Pathol; 2011; 30(6):355-8. PubMed ID: 21895521
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Diagnosis oligohydramnios-related pulmonary hypoplasia (Potter syndrome): value of portable voiding cystourethrography in newborns with respiratory distress.
    Wolf EL; Berdon WE; Baker DH; Wigger HJ; Blanc WA
    Radiology; 1977 Dec; 125(3):769-73. PubMed ID: 928707
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts.
    Tüysüz B; Zeybek C; Zorer G; Sipahi O; Ungür S
    Am J Med Genet; 2002 May; 109(3):206-10. PubMed ID: 11977180
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Autopsy findings in a stillborn female infant with the Osebold-Remondini syndrome.
    Opitz JM; Gilbert EF
    Am J Med Genet; 1985 Dec; 22(4):811-9. PubMed ID: 4073129
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Rubinstein-Taybi syndrome (a propos of 4 cases)].
    Levy-Leblond E; D'Oelsnitz M; Vaillant JM; Maroteaux P
    Arch Fr Pediatr; 1969 May; 26(5):523-35. PubMed ID: 5363526
    [No Abstract]   [Full Text] [Related]  

  • 38. A female patient with neurological, facial, digital and renal abnormalities: another case of the neurofaciodigitorenal (NFDR) syndrome?
    Rump P; Gruijters MY; Van der Burgt CJ
    Clin Dysmorphol; 1997 Oct; 6(4):337-40. PubMed ID: 9354842
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Popliteal pterygium syndrome.
    Herold HZ; Shmueli G; Baruchin AM
    Clin Orthop Relat Res; 1986 Aug; (209):194-7. PubMed ID: 3731594
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Distal limb deficiencies, oral involvement, and renal defect: report of a third patient and confirmation of a distinct entity.
    Keymolen K; Van Damme-Lombaerts R; Verloes A; Fryns JP
    Am J Med Genet; 2000 Jul; 93(1):19-21. PubMed ID: 10861677
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.