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 *

96 related articles for article (PubMed ID: 1787996)

  • 21. Prenatal diagnosis of interstitial deletion of 17(p11.2p11.2) (Smith-Magenis syndrome).
    Fan YS; Farrell SA
    Am J Med Genet; 1994 Jan; 49(2):253-4. PubMed ID: 8116679
    [No Abstract]   [Full Text] [Related]  

  • 22. Prenatal diagnosis of a congenital anomaly of isochromosome 18q--a case report.
    Shyu SK; Yang ML; Ng HT; Hsu I; Wang JS; Ho DM
    Zhonghua Yi Xue Za Zhi (Taipei); 1988 May; 41(5):383-8. PubMed ID: 3219651
    [No Abstract]   [Full Text] [Related]  

  • 23. [2 new cases of deletion of the short arm of chromosome 9].
    Antonenko VG; Demintseva VS; Demina NA; Levina LIa
    Pediatriia; 1987; (3):81-4. PubMed ID: 3601545
    [No Abstract]   [Full Text] [Related]  

  • 24. Vertical transmission of the Ohdo blepharophimosis syndrome.
    Mhanni AA; Dawson AJ; Chudley AE
    Am J Med Genet; 1998 May; 77(2):144-8. PubMed ID: 9605288
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
    Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Genetic syndromes of multiple congenital developmental defects].
    Laziuk GI; Lur'e IV; Cherstvoĭ ED
    Arkh Patol; 1977; 39(3):3-11. PubMed ID: 193472
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [A new clinico-cytogenetic syndrome--a proximal deletion of the short arm of chromosome 17].
    Zaletaev DV; Marincheva GS
    Pediatriia; 1988; (11):82-4. PubMed ID: 3226810
    [No Abstract]   [Full Text] [Related]  

  • 28. Abnormal clavicles in a neonate with partial monosomy 21.
    Wang SH; Aftimos S
    Pediatr Radiol; 1999 Mar; 29(3):221-2. PubMed ID: 10201044
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Tetrasomy 9p caused by idic (9) (pter----q13----pter).
    Cavalcanti DP; Ferrari I; de Almeida JC; de Pina Neto JM; de Oliveira JA
    Am J Med Genet; 1987 Jul; 27(3):497-503. PubMed ID: 3631125
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Constitutional chromosome anomalies in patients with cerebral gigantism (Sotos syndrome).
    Haeusler G; Guchev Z; Köhler I; Schober E; Haas O; Frisch H
    Klin Padiatr; 1993; 205(5):351-3. PubMed ID: 8411901
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
    Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Trisomy 16p in a liveborn infant and review of trisomy 16p.
    O'Connor TA; Higgins RR
    Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
    van Buggenhout G; Decock P; Fryns JP
    Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Chromosomal syndromes in the autosomal system and the problems of differential diagnosis].
    Grechanina EIa; Pesochina EA; Babadzhanian EN; Bondarenko AV
    Tsitol Genet; 1993; 27(4):61-6. PubMed ID: 8249166
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
    De Pater JM; Van Tintelen JP; Stigter R; Brouwers HA; Scheres JM
    Genet Couns; 2000; 11(3):241-7. PubMed ID: 11043432
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
    Petty EM; Gibson LH; Breg WR; Burns JP; Yang-Feng TL
    Am J Med Genet; 1993 Mar; 45(6):770-3. PubMed ID: 8456860
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
    Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [The chromosome bands. Significance for clinical and cytogenetic research (author's transl)].
    Stengel-Rutkowski S; Walther JU; Wirtz A; Frankenberger R; Albert A; Murken JD
    MMW Munch Med Wochenschr; 1976 May; 118(19):595-608. PubMed ID: 59310
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Fetal phenotypic aspects of trisomy 18. 9 cases diagnosed prenatally].
    Doria Lamba Carbone L; Pierluigi M; Camera G; Dagna Bricarelli F
    Pathologica; 1985; 77(1052):743-55. PubMed ID: 3842996
    [No Abstract]   [Full Text] [Related]  

  • 40. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
    Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.