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 *

73 related articles for article (PubMed ID: 2801771)

  • 1. Apparently previously undescribed X-linked dominant syndrome with facial and skeletal anomalies.
    Kapur S; Swinford A; Freimanis AK; Lachman RS
    Am J Med Genet; 1989 Jul; 33(3):357-63. PubMed ID: 2801771
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Omphalocele and multiple severe congenital anomalies associated with osteodysplasty (Melnick-Needles syndrome).
    von Oeyen P; Holmes LB; Trelstad RL; Griscom NT
    Am J Med Genet; 1982 Dec; 13(4):453-63. PubMed ID: 7158644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The thoracoabdominal syndrome (TAS): a new X-linked dominant disorder.
    Carmi R; Barbash A; Mares AJ
    Am J Med Genet; 1990 May; 36(1):109-14. PubMed ID: 2139758
    [TBL] [Abstract][Full Text] [Related]  

  • 4. W syndrome: report of three cases and review.
    Goizet C; Bonneau D; Lacombe D
    Am J Med Genet; 1999 Dec; 87(5):446-9. PubMed ID: 10594887
    [TBL] [Abstract][Full Text] [Related]  

  • 5. X-linked or autosomal dominant, lethal in the male, inheritance of the Melnick-Needles (osteodysplasty) syndrome? A reappraisal.
    Gorlin RJ; Knier J
    Am J Med Genet; 1982 Dec; 13(4):465-7. PubMed ID: 7158645
    [No Abstract]   [Full Text] [Related]  

  • 6. Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosis.
    Opitz JM; Mollica F; Sorge G; Milana G; Cimino G; Caltabiano M
    Am J Med Genet; 1993 Oct; 47(5):660-78. PubMed ID: 8266994
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.
    Chudley AE; Lowry RB; Hoar DI
    Am J Med Genet; 1988 Dec; 31(4):741-51. PubMed ID: 3239563
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.
    Lacombe D; Bonneau D; Verloes A; Couet D; Koulischer L; Battin J
    Genet Couns; 1993; 4(3):193-8. PubMed ID: 8267926
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia.
    Wieacker P; Wolff G; Wienker TF; Sauer M
    Am J Med Genet; 1985 Apr; 20(4):597-606. PubMed ID: 4039531
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS; Wisniewski K; Brown WT
    Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    Ng D; Hadley DW; Tifft CJ; Biesecker LG
    Am J Med Genet; 2002 Jul; 110(4):308-14. PubMed ID: 12116202
    [TBL] [Abstract][Full Text] [Related]  

  • 12. XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome).
    Sutphen R; Amar MJ; Kousseff BG; Toomey KE
    Am J Med Genet; 1995 Jul; 57(3):489-92. PubMed ID: 7677157
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital hypotrichosis and milia: report of a large family suggesting X-linked dominant inheritance.
    Rapelanoro R; Taïeb A; Lacombe D
    Am J Med Genet; 1994 Oct; 52(4):487-90. PubMed ID: 7747764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Anterior segment anomalies of the eye, clefting and skeletal abnormalities in two sibs of consanguineous parents: Michels syndrome or new syndrome?
    al Gazali LI; al Talabani J; Mosawi A; Lytle W
    Clin Dysmorphol; 1994 Jul; 3(3):238-44. PubMed ID: 7981860
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).
    Gibbons RJ; Brueton L; Buckle VJ; Burn J; Clayton-Smith J; Davison BC; Gardner RJ; Homfray T; Kearney L; Kingston HM
    Am J Med Genet; 1995 Jan; 55(3):288-99. PubMed ID: 7726225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome.
    al-Gazali LI; Bakir M; Sadaghatian MR; Nath R; Haas D
    Clin Dysmorphol; 1999 Apr; 8(2):87-92. PubMed ID: 10319196
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French family.
    Lefort G; Taib J; Toutain A; Houdayer C; Moraine CI; Humeau C; Sarda P
    Ann Genet; 1993; 36(4):200-5. PubMed ID: 8166424
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A previously unreported, dominantly inherited syndrome of shortness of stature, ear malformations, and hip dislocation: the coxoauricular syndrome--autosomal or X-linked male-lethal.
    Duca D; Pană I; Ciovirnache M; Simionesu L; Ispas I; Maxililian C
    Am J Med Genet; 1981; 8(2):173-80. PubMed ID: 7282772
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Noonan syndrome or new autosomal dominant condition with coarctation of the aorta, hypertrophic cardiomyopathy, and minor anomalies.
    Lemire EG
    Am J Med Genet; 2002 Dec; 113(3):286-90. PubMed ID: 12439898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Borjeson-Forssman-Lehmann syndrome. A family study.
    Dereymaeker AM; Fryns JP; Hoefnagels M; Heremans G; Marien J; van den Berghe H
    Clin Genet; 1986 Apr; 29(4):317-20. PubMed ID: 3720009
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.