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 *

85 related articles for article (PubMed ID: 2275296)

  • 21. The basal cell naevus syndrome. Report of a family with anosmia and a case of hypogonadotrophic hypopituitarism.
    Wallace DC; Murphy KJ; Kelly L; Ward WH
    J Med Genet; 1973 Mar; 10(1):30-3. PubMed ID: 4697853
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Klinefelter's syndrome and the XYY syndrome. A genetical, endocrinological and psychiatric-psychological study of thirty-three severely hypogonadal male patients and two patients with karyotype 47,XYY.
    Nielsen J
    Acta Psychiatr Scand Suppl; 1969; 209():1-353. PubMed ID: 5264100
    [No Abstract]   [Full Text] [Related]  

  • 23. Klinefelter's syndrome and the XXY syndrome. A genetical, endocrinological and psychiatric-psychological study of thirty-three severely hypogonadal male patients and two patients with karyotype 47,XYY.
    Nielsen J
    Acta Psychiatr Scand Suppl; 1969; 209():1-353. PubMed ID: 5263344
    [No Abstract]   [Full Text] [Related]  

  • 24. [Smith-Magenis syndrome: a case report].
    Quijano Roy S; Delicado Navarro A; López Pajares I; Pascual-Castroviejo I
    An Esp Pediatr; 1998 Oct; 49(4):405-8. PubMed ID: 9859558
    [No Abstract]   [Full Text] [Related]  

  • 25. [Syndrome 49,XXXXY,9qh+. Case report].
    Rocca M; Vivalda L; Bossi B; Spada M
    Minerva Pediatr; 1994 Apr; 46(4):165-8. PubMed ID: 8084325
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The Rud syndrome: ichthyosis, hypogonadism, mental retardation.
    Nissley PS; Thomas GH
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):246-7. PubMed ID: 5173271
    [No Abstract]   [Full Text] [Related]  

  • 27. [Mosaic variant of the translocation form of syndrome 18q-].
    Badalian LO; Dement'eva GM; Malygina NA; Mutovin GR; Petrukhin AS
    Genetika; 1981; 17(10):1867-71. PubMed ID: 7198075
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Primary gonadal hypoplasia and dysmorphic features in ring chromosome 15 syndrome.
    László J; Gaál M; Bösze P
    Clin Genet; 1982 May; 21(5):351. PubMed ID: 7116681
    [No Abstract]   [Full Text] [Related]  

  • 29. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE; Appadorai V; Breg WR; Howard RO
    Birth Defects Orig Artic Ser; 1974; 10(8):19-25. PubMed ID: 4142400
    [No Abstract]   [Full Text] [Related]  

  • 30. [Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression].
    Stoll C; Roth MP; Hessemann H; Paira M
    Arch Fr Pediatr; 1983 Dec; 40(10):763-6. PubMed ID: 6673680
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Structure and karyotype in male gonadal pathology. (Review and personal contribution)].
    Frajese G; Savioli M
    Folia Endocrinol; 1970 Feb; 23(1):46-59. PubMed ID: 5537052
    [No Abstract]   [Full Text] [Related]  

  • 32. [Potter's syndrome and polycystic kidney in the newborn].
    Pasquier B; Couderc P; Bost M; Rambaud P
    Sem Hop; 1971 Dec; 47(49):2779-88. PubMed ID: 4335740
    [No Abstract]   [Full Text] [Related]  

  • 33. [Tetrasomy 18p: report of a case].
    Borrego López S; Nieto Barrera M; Antiñolo Gil G; Sánchez García J; de la Rosa Oliver A
    An Esp Pediatr; 1988 Jul; 29(1):80-2. PubMed ID: 3056147
    [No Abstract]   [Full Text] [Related]  

  • 34. Chromosome study of the family with a daughter showing 9p+ syndrome.
    Santadusit A; Wangpreedalertkul W; Anusri Y; Meevatee U
    J Med Assoc Thai; 1981 Sep; 64(9):480-4. PubMed ID: 7299300
    [No Abstract]   [Full Text] [Related]  

  • 35. Isochromosome 18p in a mother and her child.
    Abeliovich D; Dagan J; Levy A; Steinberg A; Zlotogora J
    Am J Med Genet; 1993 Jun; 46(4):392-3. PubMed ID: 8357009
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Studies of the chromosome pattern in Stein-Leventhal syndrome].
    Lezhava TA
    Tsitologiia; 1966; 8(2):221-9. PubMed ID: 5984071
    [No Abstract]   [Full Text] [Related]  

  • 37. Brief clinical report: the dup(17p) syndrome.
    Feldman GM; Baumer JG; Sparkes RS
    Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [A case of neonatal Pallister-Killian syndrome (tetrasomy 12p)].
    González de Dios J; García-Alix Pérez A; Díaz de Bustamante A; Delicado Navarro A; Arés Segura S; Salas Hernández S; Quero Jiménez J
    An Esp Pediatr; 1993 Mar; 38(3):277-9. PubMed ID: 8460851
    [No Abstract]   [Full Text] [Related]  

  • 39. Woodhouse-Sakati syndrome: case report and symptoms review.
    Medica I; Sepcić J; Peterlin B
    Genet Couns; 2007; 18(2):227-31. PubMed ID: 17710875
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
    [No Abstract]   [Full Text] [Related]  

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