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 *

149 related articles for article (PubMed ID: 5454728)

  • 21. [Aarskog's facio-digital-genital syndrome. Clinical contribution].
    Larpi P; Savanelli A; Cigliano B; De Fazio P; Vecchio P; Esposito P
    Minerva Chir; 1985 Dec 15-31; 40(23-24):1689-92. PubMed ID: 2870446
    [No Abstract]   [Full Text] [Related]  

  • 22. Cerebro-reno-digital syndrome in two sibs.
    Piantanida M; Tiberti A; Plebani A; Martelli P; Danesino C
    Am J Med Genet; 1993 Sep; 47(3):420-2. PubMed ID: 8135292
    [TBL] [Abstract][Full Text] [Related]  

  • 23. OFD I syndrome and mental retardation.
    Yeamans EH
    Cleft Palate J; 1973 Jan; 10():84-91. PubMed ID: 4509409
    [No Abstract]   [Full Text] [Related]  

  • 24. [The orofaciodigital syndrome. The Papillon-Léage-Psaume syndrome].
    Koberg W; Schettler D
    Dtsch Zahnarztl Z; 1969; 24(11):1002-7. PubMed ID: 5261935
    [No Abstract]   [Full Text] [Related]  

  • 25. [Coffin-Lowry syndrome. Description of 2 cases].
    Barajas LO; Rivera H; Fragoso R; Nazara Z; Cantú JM
    Bol Med Hosp Infant Mex; 1986 Jun; 43(6):378-81. PubMed ID: 3730116
    [No Abstract]   [Full Text] [Related]  

  • 26. [Orofaciodigital syndrome. Clinical features and genetics].
    Stahl A; Furhmann W
    Dtsch Med Wochenschr; 1968 Jun; 93(25):1224-8. PubMed ID: 4298244
    [No Abstract]   [Full Text] [Related]  

  • 27. [Papillon=Léage-Psaume syndrome. 4 cases of dysostosis orodigitofacialis].
    Koberg W; Schettler D
    Z Kinderheilkd; 1966; 96(2):147-62. PubMed ID: 5982667
    [No Abstract]   [Full Text] [Related]  

  • 28. Coffin-Lowry syndrome in an Afro-American family.
    Kousseff BG
    Am J Med Genet; 1982 Mar; 11(3):373-5. PubMed ID: 7081302
    [No Abstract]   [Full Text] [Related]  

  • 29. [Orofaciodigital syndrome type I in a mother and daughter].
    Guerrero Vázquez J; Cazenave Bernal A; de Paz Aparicio P; Luengo Casasola JL; Garcés Ramos A; López Vázquez JL; Hoyos Madrid JJ
    An Esp Pediatr; 1988 Jan; 28(1):59-62. PubMed ID: 3279888
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Brachmann-de Lange syndrome: report of 4 cases in Mexican children].
    Villegas-Camargo I; Lacro RV; Lyons-Jones K
    Bol Med Hosp Infant Mex; 1987 Dec; 44(12):766-70. PubMed ID: 3426781
    [No Abstract]   [Full Text] [Related]  

  • 31. [Oro-facial-digital syndrome II: report of a case and differential diagnosis from similar clinical pictures].
    Borrego López S; Antiñolo Gil G; Cañadas García de León M; Villar Rodríguez JL
    An Esp Pediatr; 1989 Nov; 31(5):489-91. PubMed ID: 2619139
    [No Abstract]   [Full Text] [Related]  

  • 32. [Pediatric dentistry syndrome with various oro-systemic congenital abnormalities (condroectodermal dysplasia or oro-digital-facial disorders); presentation of a case].
    Menendez OR; Perez ER
    Cent Estud Recur Odontol Nino; 1981 Apr; 6(1):45-50. PubMed ID: 6942943
    [No Abstract]   [Full Text] [Related]  

  • 33. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E; Palmieri A; Bertola A; Bellini C
    Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Japanese kindred with FG syndrome.
    Kato R; Niikawa N; Nagai T; Fukushima Y
    Am J Med Genet; 1994 Aug; 52(2):242-3. PubMed ID: 7802020
    [No Abstract]   [Full Text] [Related]  

  • 35. [Papillon-Léage-Psaume type I oro-facio-digital syndrome. Apropos of a case].
    Galabert J; Bourdoncle A
    Actual Odontostomatol (Paris); 1984 Dec; 38(148):745-54. PubMed ID: 6599378
    [No Abstract]   [Full Text] [Related]  

  • 36. [Considerations on lipomatosis of the tongue in the framework of orofaciodigital syndrome].
    Berger PE; Dambrain R; Peiffer R
    Acta Stomatol Belg; 1967; 64(2):207-31. PubMed ID: 4861315
    [No Abstract]   [Full Text] [Related]  

  • 37. [Aarskog's syndrome. Description of a familial case].
    Tucciarone L; De Santis F; Ballati G; Latini M; Felici W
    Minerva Pediatr; 1987 Apr; 39(8):341-6. PubMed ID: 3614163
    [No Abstract]   [Full Text] [Related]  

  • 38. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.
    Reardon W; Gibbons RJ; Winter RM; Baraitser M
    Am J Med Genet; 1995 Jan; 55(3):285-7. PubMed ID: 7726224
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.
    Sadler LS; Robinson LK
    Am J Med Genet; 1993 Aug; 47(1):65-8. PubMed ID: 8368255
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Pilosebaceous dysplasia in the oral-facial-digital syndrome.
    Solomon LM; Fretzin D; Pruzansky S
    Arch Dermatol; 1970 Dec; 102(6):598-602. PubMed ID: 5501900
    [No Abstract]   [Full Text] [Related]  

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