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 *

285 related articles for article (PubMed ID: 1632438)

  • 41. "Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred.
    Jackson CE; Weiss L; Watson JH
    Pediatrics; 1974 Aug; 54(2):201-7. PubMed ID: 4847854
    [No Abstract]   [Full Text] [Related]  

  • 42. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
    Martínez-Frías ML; Martín M; Pardo M; Fernandez de las Heras F; Frías JL
    Am J Med Genet; 1995 Jan; 55(2):213-6. PubMed ID: 7717420
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Acro-renal-mandibular syndrome.
    Halal F; Desgranges MF; Leduc B; Thêorét G; Bettez P
    Am J Med Genet; 1980; 5(3):277-84. PubMed ID: 7405959
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E; Clemens M
    Am J Med Genet; 1996 Mar; 62(1):58-60. PubMed ID: 8779326
    [TBL] [Abstract][Full Text] [Related]  

  • 46. New form of postaxial acrofacial dysostosis?
    Arens R; Reichman B; Katznelson MB; Goodman RM
    Am J Med Genet; 1991 Dec; 41(4):438-43. PubMed ID: 1776633
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Dysmorphology report holoprosencephaly-polydactyly syndrome: affected brother and sister with a wide spectrum of anomalies.
    Delozier-Blanchet CD; Engel E
    Genet Couns; 1992; 3(1):57-8. PubMed ID: 1590983
    [No Abstract]   [Full Text] [Related]  

  • 49. Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from Montana.
    Opitz JM; Lowry RB; Holmes TM; Morgan K
    Am J Med Genet; 1985 Nov; 22(3):521-9. PubMed ID: 4061488
    [TBL] [Abstract][Full Text] [Related]  

  • 50. McKusick-Kaufman syndrome: report of the 66th case complicated by a staphyloma of the left eye.
    Cantani A; Santillo C; Cozzi F
    Padiatr Padol; 1991; 26(4):193-6. PubMed ID: 1749628
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?
    Kotzot D; Richter K; Gierth-Fiebig K
    Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Short stature, abnormal ears, monodactylous tetraectrodactyly, cleft palate in a Brazilian boy.
    Richieri-Costa A; de Miranda E
    Am J Med Genet; 1988 Nov; 31(3):559-64. PubMed ID: 3228138
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
    Børglum AD; Balslev T; Haagerup A; Birkebaek N; Binderup H; Kruse TA; Hertz JM
    Eur J Hum Genet; 2001 Oct; 9(10):753-7. PubMed ID: 11781686
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents.
    Richieri-Costa A; Pirolo Júnior L; Cohen MM
    Am J Med Genet; 1993 Aug; 47(2):281-3. PubMed ID: 8213921
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Autosomal recessive form of whistling face syndrome in sibs.
    Dallapiccola B; Giannotti A; Lembo A; Saguì L
    Am J Med Genet; 1989 Aug; 33(4):542-4. PubMed ID: 2596515
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC; Geerdink RA; Hamel BC; Hennekam FA; Kraus P; Rammeloo JA; Tillemans AA
    Am J Med Genet; 1989 Dec; 34(4):593-600. PubMed ID: 2624276
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A new short rib syndrome: report of two cases.
    Beemer FA; Langer LO; Klep-de Pater JM; Hemmes AM; Bylsma JB; Pauli RM; Myers TL; Haws CC
    Am J Med Genet; 1983 Jan; 14(1):115-23. PubMed ID: 6829599
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Marden-Walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consanguineous parents.
    van den Ende JJ; van Bever Y; Rodini ES; Richieri-Costa A
    Am J Med Genet; 1992 Feb; 42(4):467-9. PubMed ID: 1609830
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Autosomal recessive acrorenal syndrome.
    Miltényi M; Czeizel AE; Balogh L; Detre Z
    Am J Med Genet; 1992 Jul; 43(5):789-90. PubMed ID: 1344975
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphy.
    Stoll C; Finck S; Janser B; Printz M; Lutz P
    Genet Couns; 1992; 3(1):41-7. PubMed ID: 1590980
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.