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 *

104 related articles for article (PubMed ID: 1628682)

  • 1. Male triplets concordant for X-linked recessive nonsyndromic hypoparathyroidism.
    Teebi AS; Kishawi AR; Malek AH
    Eur J Pediatr; 1992 Jun; 151(6):468. PubMed ID: 1628682
    [No Abstract]   [Full Text] [Related]  

  • 2. Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.
    Thakker RV; Davies KE; Whyte MP; Wooding C; O'Riordan JL
    J Clin Invest; 1990 Jul; 86(1):40-5. PubMed ID: 1973175
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.
    Trump D; Dixon PH; Mumm S; Wooding C; Davies KE; Schlessinger D; Whyte MP; Thakker RV
    J Med Genet; 1998 Nov; 35(11):905-9. PubMed ID: 9832036
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Idiopathic hypoparathyroidism presenting with seizures during infancy: X-linked recessive inheritance in a large Missouri kindred.
    Whyte MP; Weldon VV
    J Pediatr; 1981 Oct; 99(4):608-11. PubMed ID: 7196945
    [No Abstract]   [Full Text] [Related]  

  • 5. Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy.
    Dahlberg PJ; Borer WZ; Newcomer KL; Yutuc WR
    Am J Med Genet; 1983 Sep; 16(1):99-104. PubMed ID: 6638075
    [TBL] [Abstract][Full Text] [Related]  

  • 6. mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.
    Mumm S; Whyte MP; Thakker RV; Buetow KH; Schlessinger D
    Am J Hum Genet; 1997 Jan; 60(1):153-9. PubMed ID: 8981958
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Absence of parathyroid tissue in sex-linked recessive hypoparathyroidism.
    Whyte MP; Kim GS; Kosanovich M
    J Pediatr; 1986 Nov; 109(5):915. PubMed ID: 3772677
    [No Abstract]   [Full Text] [Related]  

  • 8. Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay.
    Shaw NJ; Haigh D; Lealmann GT; Karbani G; Brocklebank JT; Dillon MJ
    Arch Dis Child; 1991 Oct; 66(10):1191-4. PubMed ID: 1719942
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and genetic heterogeneity in idiopathic Addison's disease and hypoparathyroidism.
    Spinner MW; Blizzard RM; Childs B
    J Clin Endocrinol Metab; 1968 Jun; 28(6):795-804. PubMed ID: 5656437
    [No Abstract]   [Full Text] [Related]  

  • 10. Familial Hirschsprung's disease: report of autosomal dominant and probable recessive X-linked kindreds.
    Stannard VA; Fowler C; Robinson L; Besner G; Glick PL; Allen JE; Jewett TC; Cooney DR
    J Pediatr Surg; 1991 May; 26(5):591-4. PubMed ID: 2061816
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial idiopathic hypoparathyroidism.
    Bronsky D; Kiamko RT; Waldstein SS
    J Clin Endocrinol Metab; 1968 Jan; 28(1):61-5. PubMed ID: 5635448
    [No Abstract]   [Full Text] [Related]  

  • 12. Evidence of a third locus in X-linked recessive spastic paraplegia.
    Steinmüller R; Lantigua-Cruz A; Garcia-Garcia R; Kostrzewa M; Steinberger D; Müller U
    Hum Genet; 1997 Aug; 100(2):287-9. PubMed ID: 9254866
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exclusion of close linkage between the parathyroid hormone gene and a mutant gene locus causing idiopathic hypoparathyroidism.
    Schmidtke J; Kruse K; Pape B; Sippell G
    J Med Genet; 1986 Jun; 23(3):217-9. PubMed ID: 3014148
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X-linked recessive myotubular myopathy proven by muscle biopsy.
    Tsai CH; Huang WS; Tsai FJ; Lee CC; Chen SS
    J Formos Med Assoc; 1996 Feb; 95(2):153-6. PubMed ID: 9064005
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paediatric aspects of hypoparathyroidism.
    MacGregor ME
    Proc R Soc Med; 1968 Jun; 61(6):583-8. PubMed ID: 5690849
    [No Abstract]   [Full Text] [Related]  

  • 16. A family showing apparent X linked inheritance of both anencephaly and spina bifida.
    Jensson O; Arnason A; Gunnarsdottir H; Petursdottir I; Fossdal R; Hreidarsson S
    J Med Genet; 1988 Apr; 25(4):227-9. PubMed ID: 3285008
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel Fryns "Anophthalmia-plus" syndrome associated with primary hypothyroidism.
    Akalin I; Senses DA; Ilgin-Ruhi H; Misirlioğlu E; Yalçiner M; Cetinkaya E; Fryns JP; Tükün A
    Genet Couns; 2005; 16(2):145-8. PubMed ID: 16080293
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Five siblings of familial idiopathic hypoparathyroidism].
    Uchida M; Son T; Miura R
    Rinsho Shinkeigaku; 1983 Mar; 23(3):235-41. PubMed ID: 6872380
    [No Abstract]   [Full Text] [Related]  

  • 19. X-linked infantile spinal muscular atrophy.
    Greenberg F; Fenolio KR; Hejtmancik JF; Armstrong D; Willis JK; Shapira E; Huntington HW; Haun RL
    Am J Dis Child; 1988 Feb; 142(2):217-9. PubMed ID: 3341327
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A ring chromosome No. 16 in an infant with primary hypoparathyroidism.
    Pergament E; Pietra GC; Kadotani T; Sato H; Berlow S
    J Pediatr; 1970 May; 76(5):745-51. PubMed ID: 5440360
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.