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 *

143 related articles for article (PubMed ID: 6407320)

  • 1. Autosomal dominant partial lipodystrophy associated with Rieger anomaly, short stature, and insulinopenic diabetes.
    Aarskog D; Ose L; Pande H; Eide N
    Am J Med Genet; 1983 May; 15(1):29-38. PubMed ID: 6407320
    [TBL] [Abstract][Full Text] [Related]  

  • 2. SHORT syndrome: a new case with probable autosomal dominant inheritance.
    Sorge G; Ruggieri M; Polizzi A; Scuderi A; Di Pietro M
    Am J Med Genet; 1996 Jan; 61(2):178-81. PubMed ID: 8669449
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial lipoatrophic diabetes with dominant transmission. A new syndrome.
    Dunnigan MG; Cochrane MA; Kelly A; Scott JW
    Q J Med; 1974 Jan; 43(169):33-48. PubMed ID: 4362786
    [No Abstract]   [Full Text] [Related]  

  • 4. [The Rieger syndrome. A clinical study. A study of 4 generations in one family with the Rieger syndrome].
    Rusu V
    Oftalmologia; 1997; 41(3):234-7. PubMed ID: 9409970
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case report on SHORT syndrome.
    Joo SH; Raygada M; Gibney S; Farzaneh I; Rennert OM
    Clin Dysmorphol; 1999 Jul; 8(3):219-21. PubMed ID: 10457859
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical, endocrine and metabolic studies in the kindred of familial partial lipodystrophy--a syndrome of insulin resistance.
    Vaidya RA; Vaidya AD; Talwalkar SC; Mehtalia SD; Shringi MS; Pandey SN; Shah SJ; Godse C; Joshi JV; Sheth J; Kamdar VV
    J Assoc Physicians India; 2002 Jun; 50():773-6. PubMed ID: 12240840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22.
    Peters JM; Barnes R; Bennett L; Gitomer WM; Bowcock AM; Garg A
    Nat Genet; 1998 Mar; 18(3):292-5. PubMed ID: 9500556
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal dominant inheritance of the Aarskog syndrome.
    Grier RE; Farrington FH; Kendig R; Mamunes P
    Am J Med Genet; 1983 May; 15(1):39-46. PubMed ID: 6344635
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: a new autosomal dominant syndrome.
    Stern JK; Lubinsky MS; Durrie DS; Luckasen JR
    Am J Med Genet; 1984 May; 18(1):67-77. PubMed ID: 6234802
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GMS syndrome: a new dominant condition with goniodysgenesis, mental retardation, and short stature.
    Kupchik GS; Ludman MD; Raab EL; Gilbert F
    Am J Med Genet; 1992 Jan; 42(1):1-4. PubMed ID: 1308345
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Okihiro syndrome: thenar hypoplasia and Duane anomaly in three generations.
    Collins A; Baraitser M; Pembrey M
    Clin Dysmorphol; 1993 Jul; 2(3):237-40. PubMed ID: 8287186
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Report of a case and further delineation of the SHORT syndrome.
    Toriello HV; Wakefield S; Komar K; Higgins JV; Waterman DF
    Am J Med Genet; 1985 Oct; 22(2):311-4. PubMed ID: 4050863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
    Ibsen HH; Clemmensen OJ; Brandrup F
    Acta Derm Venereol; 1991; 71(4):349-51. PubMed ID: 1681656
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lipodystrophy of the extremities. A dominantly inherited syndrome associated with lipatrophic diabetes.
    Köbberling J; Willms B; Kattermann R; Creutzfeldt W
    Humangenetik; 1975 Sep; 29(2):111-20. PubMed ID: 170190
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.
    Komatireddy S; Chakrabarti S; Mandal AK; Reddy AB; Sampath S; Panicker SG; Balasubramanian D
    Mol Vis; 2003 Feb; 9():43-8. PubMed ID: 12592227
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cataracts, motor system disorder, short stature, learning difficulties, and skeletal abnormalities: a new syndrome?
    Slavotinek AM; Pike M; Mills K; Hurst JA
    Am J Med Genet; 1996 Mar; 62(1):42-7. PubMed ID: 8779323
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ruvalcaba syndrome: autosomal dominant inheritance.
    Sugio Y; Kajii T
    Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face.
    Winter RM
    Am J Med Genet; 1993 Nov; 47(6):917-20. PubMed ID: 7506485
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome.
    Morava E; Czakó M; Kárteszi J; Cser B; Weissbecker K; Méhes K
    Clin Dysmorphol; 2003 Jul; 12(3):161-5. PubMed ID: 14564152
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dominant inheritance of microcephaly, short stature and congenital dislocation of the hips.
    Newbury-Ecob RA; Young ID
    Clin Dysmorphol; 1993 Jan; 2(1):34-8. PubMed ID: 8298736
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.