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 *

118 related articles for article (PubMed ID: 890099)

  • 1. Acrofacial dysostosis with growth and mental retardation in three males, one with simultaneous Hermansky-Pudlak syndrome.
    Kelly TE; Cooke RJ; Kester RW
    Birth Defects Orig Artic Ser; 1977; 13(3B):45-52. PubMed ID: 890099
    [No Abstract]   [Full Text] [Related]  

  • 2. [Partial 11q monosomy and trigonocephaly. A new syndrome].
    Turleau C; Chavin-Colin F; Roubin M; Thomas D; de Grouchy TJ
    Ann Genet; 1975 Dec; 18(4):257-60. PubMed ID: 1083197
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Trisomy 4p. A case presentation (author's transl)].
    Delgado A; Egüés J; Muñoz M; González Villa P; Bernaola E; del Amo A
    An Esp Pediatr; 1981 Oct; 15(4):383-9. PubMed ID: 7337304
    [No Abstract]   [Full Text] [Related]  

  • 4. Postaxial acrofacial dysostosis syndrome with microcephaly, seizures and profound mental retardation.
    Hauss-Albert H; Passarge E
    Am J Med Genet; 1988 Nov; 31(3):701-3. PubMed ID: 3228151
    [No Abstract]   [Full Text] [Related]  

  • 5. Association of hypertelorism and hypospadias--the BBB-syndrome.
    Michaelis E; Mortier W
    Helv Paediatr Acta; 1972 Dec; 27(6):575-81. PubMed ID: 4405408
    [No Abstract]   [Full Text] [Related]  

  • 6. Ring chromosome 15 syndrome.
    Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H
    Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144
    [No Abstract]   [Full Text] [Related]  

  • 7. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL; Morlier BG; Roux C
    Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Albinism and the Hermanský-Pudlák syndrome (author's transl)].
    Cieslar P; Smetana K; Matousová O
    Cas Lek Cesk; 1976 Feb; 115(8):243-6. PubMed ID: 1253233
    [No Abstract]   [Full Text] [Related]  

  • 9. Short stature, mental retardation and ocular alterations in three siblings.
    Mollica F; Pavone L; Antener I
    Helv Paediatr Acta; 1972 Nov; 27(5):463-9. PubMed ID: 4640901
    [No Abstract]   [Full Text] [Related]  

  • 10. [Identification of the small submetacentric supernumerary chromosome in the cat's-eye syndrome].
    Noël B; Mottet J; Nantois Y; Quack B
    J Genet Hum; 1973 Mar; 21(1):23-32. PubMed ID: 4742121
    [No Abstract]   [Full Text] [Related]  

  • 11. The leopard (multiple lentigines) syndrome revisited.
    Gorlin RJ; Anderson RC; Moller JH
    Laryngoscope; 1971 Oct; 81(10):1674-81. PubMed ID: 4398858
    [No Abstract]   [Full Text] [Related]  

  • 12. The 18p- syndrome. Report of five cases.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A single D chromosome in ring form in a 2-year-old girl with mental retardation].
    Morić-Petrović S; Garzicić B; Despotović M; Kalicanin P
    Srp Arh Celok Lek; 1970 Mar; 98(3):447-52. PubMed ID: 5205520
    [No Abstract]   [Full Text] [Related]  

  • 14. Pycnodysostosis: a case report.
    Lentle BC
    J Can Assoc Radiol; 1971 Sep; 22(3):210-4. PubMed ID: 5150109
    [No Abstract]   [Full Text] [Related]  

  • 15. [Hermansky-Pudlak syndrome].
    Schallreuter KU
    Hautarzt; 1989 Mar; 40(3):130-3. PubMed ID: 2654078
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The Hermansky-Pudlak syndrome and the differential diagnosis of oculocutaneous albinism (author's transl)].
    Böhles H; Skrodzki K; Geissendörfer C; Krzywanek HJ
    Klin Padiatr; 1981 Jan; 193(1):3-6. PubMed ID: 6782329
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new familial syndrome with craniofacial abnormalities, osseous defects and mental retardation.
    Grix A; Blankenship W; Peterson R; Hall B
    Birth Defects Orig Artic Ser; 1975; 11(5):107-14. PubMed ID: 1218201
    [No Abstract]   [Full Text] [Related]  

  • 18. [A familial case of 17 r ring-shaped chromosome of group E with transmission from father to son].
    Burden M; Lupaşcu E; Mărgineanu L
    Rev Med Chir Soc Med Nat Iasi; 1973; 77(2):353-7. PubMed ID: 4146973
    [No Abstract]   [Full Text] [Related]  

  • 19. Characteristics of the phenotype in oligophrenia caused by autosomal abnormalities.
    Blyumina MG; Podugol'nikova OA; Batienko GS
    Sov Genet; 1974 Sep; 8(10):1312-4. PubMed ID: 4439047
    [No Abstract]   [Full Text] [Related]  

  • 20. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV; Driscoll DJ; Ledbetter DH; Riccardi VM
    Am J Med Genet; 1981; 9(3):231-7. PubMed ID: 7025632
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.