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 *

102 related articles for article (PubMed ID: 3993676)

  • 1. Hypergonadotropic hypogonadism with congestive cardiomyopathy: an autosomal-recessive disorder?
    Malouf J; Alam S; Kanj H; Mufarrij A; Der Kaloustian VM
    Am J Med Genet; 1985 Mar; 20(3):483-9. PubMed ID: 3993676
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dilated cardiomyopathy and ovarian dysgenesis in a patient with Malouf syndrome: a case report.
    Gersak K; Strgulc M; Gorjup V; Dolenc-Strazar Z; Jurcic V; Penny DJ; Fan Y
    Mol Med Rep; 2013 Nov; 8(5):1311-4. PubMed ID: 24008991
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cataracts and testicular failure in three brothers.
    Lubinsky MS
    Am J Med Genet; 1983 Oct; 16(2):149-52. PubMed ID: 6418006
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hypergonadotropic hypogonadism with congestive cardiomyopathy.
    Witt DR
    Am J Med Genet; 1987 Apr; 26(4):983-5. PubMed ID: 2954460
    [No Abstract]   [Full Text] [Related]  

  • 5. The Alström syndrome: is it a rare or unknown disease?
    Maffei P; Munno V; Marshall JD; Scandellari C; Sicolo N
    Ann Ital Med Int; 2002; 17(4):221-8. PubMed ID: 12532560
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Familial congestive cardiomyopathy].
    Shul'ga IuD; Baru IM; Brynzevich AK
    Ter Arkh; 1983; 55(10):75-6. PubMed ID: 6359549
    [No Abstract]   [Full Text] [Related]  

  • 7. Najjar syndrome revisited.
    Thomas IT; Jewett T; Lantz P; Covitz W; Garber P; Berry MN
    Am J Med Genet; 1993 Dec; 47(8):1151-2. PubMed ID: 8291546
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypogonadotropic hypogonadism in patients with multiple congenital defects.
    Bardin CW
    Birth Defects Orig Artic Ser; 1971 May; 7(6):175-8. PubMed ID: 5317488
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial insulin resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deafness, and mental retardation.
    Boor R; Herwig J; Schrezenmeir J; Pontz BF; Schönberger W
    Am J Med Genet; 1993 Mar; 45(5):649-53. PubMed ID: 8456839
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: another new autosomal recessive syndrome from the Middle East.
    Teebi AS; Al-Awadi SA; Farag TI; Naguib KK
    Am J Med Genet; 1986 Jun; 24(2):373-8. PubMed ID: 3717216
    [No Abstract]   [Full Text] [Related]  

  • 11. Blepharophimosis-ptosis-epicanthus inversus syndrome and hypergonadotropic hypogonadism.
    Siewert AL; Stein Q; Flanagan J; Hansen KA
    Fertil Steril; 2008 Nov; 90(5):2016.e11-2. PubMed ID: 18793770
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of Malouf syndrome.
    Narahara K; Kamada M; Takahashi Y; Tsuji K; Yokoyama Y; Ninomiya S; Seino Y
    Am J Med Genet; 1992 Oct; 44(3):369-73. PubMed ID: 1488988
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected females.
    Al-Awadi SA; Farag TI; Teebi AS; Naguib K; el-Khalifa MY; Kelani Y; Al-Ansari A; Schimke RN
    Am J Med Genet; 1985 Nov; 22(3):619-22. PubMed ID: 4061495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Borjeson-Forssman-Lehmann syndrome and dilated cardiomyopathy: a previously unreported association.
    Kaplinsky E; Perandones C; Galiana MG; Fideleff H; Favaloro RR; Carlos V; Perrone SV
    Can J Cardiol; 2001 Jan; 17(1):80-3. PubMed ID: 11173318
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition.
    Davey KM; Parboosingh JS; McLeod DR; Chan A; Casey R; Ferreira P; Snyder FF; Bridge PJ; Bernier FP
    J Med Genet; 2006 May; 43(5):385-93. PubMed ID: 16055927
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gonadal (ovarian) dysgenesis in 46,XX individuals: frequency of the autosomal recessive form.
    Meyers CM; Boughman JA; Rivas M; Wilroy RS; Simpson JL
    Am J Med Genet; 1996 Jun; 63(4):518-24. PubMed ID: 8826428
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis and long-term clinical evaluation of three siblings with Alström syndrome.
    Ozgül RK; Satman I; Collin GB; Hinman EG; Marshall JD; Kocaman O; Tütüncü Y; Yilmaz T; Naggert JK
    Clin Genet; 2007 Oct; 72(4):351-6. PubMed ID: 17850632
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The molecular basis of human hypogonadotropic hypogonadism.
    Layman LC
    Mol Genet Metab; 1999 Oct; 68(2):191-9. PubMed ID: 10527669
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness.
    Amor DJ; Delatycki MB; Gardner RJ; Storey E
    Am J Med Genet; 2001 Feb; 99(1):29-33. PubMed ID: 11170090
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism.
    Bayram Y; Gulsuner S; Guran T; Abaci A; Yesil G; Gulsuner HU; Atay Z; Pierce SB; Gambin T; Lee M; Turan S; Bober E; Atik MM; Walsh T; Karaca E; Pehlivan D; Jhangiani SN; Muzny D; Bereket A; Buyukgebiz A; Boerwinkle E; Gibbs RA; King MC; Lupski JR
    J Clin Endocrinol Metab; 2015 May; 100(5):E808-14. PubMed ID: 25774885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.