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 *

134 related articles for article (PubMed ID: 8967099)

  • 41. Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalism.
    Cohn RD; Gillessen-Kaesbach G; Dobyns WB; Kahn T; Lenard HG; Voit T
    Am J Med Genet; 1996 May; 63(1):314-7. PubMed ID: 8723127
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Russell-Silver syndrome.
    Wee SA
    Dermatol Online J; 2007 Jan; 13(1):16. PubMed ID: 17511949
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Coexistence of symptomatic iron-deficiency anemia and duodenal nodular lymphoid hyperplasia due to giardiasis: case report.
    Kasirga E; Gülen H; Simşek A; Ayhan S; Yilmaz O; Ellidokuz E
    Pediatr Hematol Oncol; 2009 Jan; 26(1):57-61. PubMed ID: 19206009
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Inverted nipples in Robinow syndrome.
    Lorenzetti MH; Fryns JP
    Genet Couns; 1996; 7(1):67-9. PubMed ID: 8652091
    [TBL] [Abstract][Full Text] [Related]  

  • 45. De Sanctis-Cacchione syndrome.
    Mittal H; Mehndiratta S; Kaushik JS; Godbole T
    Indian J Dermatol Venereol Leprol; 2013; 79(6):849. PubMed ID: 24177634
    [No Abstract]   [Full Text] [Related]  

  • 46. Symbrachydactyly involving hands and feet.
    De Smet L; Fabry G; Fryns JP
    Genet Couns; 1998; 9(1):23-7. PubMed ID: 9555583
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Zinc deficit syndrome].
    Karlinskiĭ VM
    Vopr Pitan; 1980; (1):10-8. PubMed ID: 6155003
    [No Abstract]   [Full Text] [Related]  

  • 48. [The Silver-Russel syndrome].
    Sarotti M; Zilocchi C; Bianchi P; Faraci C; Marenzi C; Martinelli D; Escobar R
    Pediatr Med Chir; 1992; 14(2):227-30. PubMed ID: 1508761
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Gingival fibromatosis, short stature, border-line IQ, facial dysmorphism and hepatomegaly.
    Marakoglu I; Percin EF; Gursoy UK; Onarlioglu B; Ergur AT
    Genet Couns; 2005; 16(2):161-5. PubMed ID: 16080296
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Geophagia associated with iron-deficiency anemia, hepatosplenomegaly, hypogonadism and dwarfism. A syndrome probably associated with zinc deficiency.
    Say B; Ozsoylu S; Berkel I
    Clin Pediatr (Phila); 1969 Nov; 8(11):661-8. PubMed ID: 5259114
    [No Abstract]   [Full Text] [Related]  

  • 51. [Non-Mendelian genetics and growth. The Russel-Silver syndrome].
    del Campo Casanelles M; Pérez Jurado L
    An Esp Pediatr; 2001 Jun; 54(6):531-5. PubMed ID: 11412398
    [No Abstract]   [Full Text] [Related]  

  • 52. Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?
    Mégarbané A; Abi Moussa M
    Genet Couns; 1997; 8(2):127-32. PubMed ID: 9219011
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Ultrastructural changes in the mucosa of the small intestine in patients with geophagia (Prasad's syndrome).
    Arcasoy A; Akar N; Ors U; Delilbasi L; Karayalcin S
    J Pediatr Gastroenterol Nutr; 1990 Aug; 11(2):279-82. PubMed ID: 2395069
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Thanatophoric dwarfism: a report of two infants.
    Sehgal D; Mulenga H; Chintu C
    East Afr Med J; 1983 Oct; 60(10):713-7. PubMed ID: 6671430
    [No Abstract]   [Full Text] [Related]  

  • 55. [Zinc and zinc deficiency--a clinical review].
    Haeger K
    Lakartidningen; 1973 Sep; 70(38):3243-6. PubMed ID: 4597667
    [No Abstract]   [Full Text] [Related]  

  • 56. Hypogonadotropic hypogonadism in a female with the Johnson-McMillin syndrome.
    De Metsenaere F; Mortier G; Dhont M
    Am J Obstet Gynecol; 2004 Nov; 191(5):1728-9. PubMed ID: 15547553
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Antenatal diagnosis of Grebe syndrome in a twin pregnancy by ultrasound.
    Kulkarni ML; Kulkarni BM; Nasser PU
    Indian Pediatr; 1995 Sep; 32(9):1007-11. PubMed ID: 8935268
    [No Abstract]   [Full Text] [Related]  

  • 58. [Cohen syndrome].
    Kayashima T; Niikawa N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):477-8. PubMed ID: 11596442
    [No Abstract]   [Full Text] [Related]  

  • 59. A Peutz-Jeghers syndrome case with iron deficiency anemia and jejuno-jejunal invagination.
    Sökmen HM; Ince AT; Bölükbaş C; Kiliç G; Dalay R; Kurdaş OO
    Turk J Gastroenterol; 2003 Mar; 14(1):78-82. PubMed ID: 14593545
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy.
    Castelnau P; Le Merrer M; Diatloff-Zito C; Marquis E; Tête MJ; Robert JJ
    Eur J Pediatr; 2000 Aug; 159(8):631-3. PubMed ID: 10968248
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.