BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 2929657)

  • 41. Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.
    Niikawa N; Kuroki Y; Kajii T; Matsuura N; Ishikiriyama S; Tonoki H; Ishikawa N; Yamada Y; Fujita M; Umemoto H
    Am J Med Genet; 1988 Nov; 31(3):565-89. PubMed ID: 3067577
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Anesthetic management of a patient with Freeman-Sheldon ("whistling face") syndrome].
    Tateishi M; Imaizumi H; Namiki A; Katsuno M; Kawana S; Ujike Y
    Masui; 1986 Jul; 35(7):1114-8. PubMed ID: 3773258
    [No Abstract]   [Full Text] [Related]  

  • 43. Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance.
    Artlich A; Schwinger E; Meinecke P
    Clin Dysmorphol; 1992 Jul; 1(3):157-60. PubMed ID: 1342863
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [You make the diagnosis. Marshall syndrome].
    Freude S; Kozel-Lachmann D
    Padiatr Padol; 1991; 26(4):197-8. PubMed ID: 1749629
    [No Abstract]   [Full Text] [Related]  

  • 45. [The popliteal pterygium syndrome. A dominant autosomal malformation syndrome].
    Pfeiffer RA; Tünte W; Reinken M
    Z Kinderheilkd; 1970; 108(2):103-16. PubMed ID: 4325529
    [No Abstract]   [Full Text] [Related]  

  • 46. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P; Lefort G; Eglin MC; Rieu D; Sarda P
    Genet Couns; 1993; 4(4):289-94. PubMed ID: 8110417
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
    [No Abstract]   [Full Text] [Related]  

  • 48. The nasopalpebral lipoma-coloboma syndrome: a new autosomal dominant dysplasia-malformation syndrome with congenital nasopalpebral lipomas, eyelid colobomas, telecanthus, and maxillary hypoplasia.
    Penchaszadeh VB; Velasquez D; Arrivillaga R
    Am J Med Genet; 1982 Apr; 11(4):397-410. PubMed ID: 7091184
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.
    Santos H; Cordeiro I; Medeira A; Mendonça E; Antunes NL; Rosa FC
    Genet Couns; 1994; 5(2):187-9. PubMed ID: 7917131
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Dominant inheritance of a syndrome similar to Rubinstein-Taybi.
    Cotsirilos P; Taylor JC; Matalon R
    Am J Med Genet; 1987 Jan; 26(1):85-93. PubMed ID: 3812583
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Further delineation of the branchio-oculo-facial syndrome.
    Lin AE; Gorlin RJ; Lurie IW; Brunner HG; van der Burgt I; Naumchik IV; Rumyantseva NV; Stengel-Rutkowski S; Rosenbaum K; Meinecke P
    Am J Med Genet; 1995 Mar; 56(1):42-59. PubMed ID: 7747785
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.
    Ohdo S; Madokoro H; Sonoda T; Takei M; Yasuda H; Mori N
    J Med Genet; 1987 Oct; 24(10):609-12. PubMed ID: 3681906
    [TBL] [Abstract][Full Text] [Related]  

  • 53. New syndrome?: MCA/MR syndrome with multiple circumferential skin creases.
    Elliott AM; Ludman M; Teebi AS
    Am J Med Genet; 1996 Mar; 62(1):23-5. PubMed ID: 8779319
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [A child with Zellweger's cerebrohepatorenal syndrome].
    Govaerts L; Corstiaensen J; Bakkeren J; Trujbels F; Monnens L
    Tijdschr Kindergeneeskd; 1983 Apr; 51(2):65-7. PubMed ID: 6879587
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB; Stevens CA
    Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Syndactylia associated with multiple malformation syndromes. Observation of a new symptomatologic complex in 3 brothers].
    Garau A; Nurchi AM; Melis P; Frau G; Costa G
    Pediatr Med Chir; 1988; 10(2):227-32. PubMed ID: 2845373
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Radial ray aplasia and renal anomalies in father and son: a new syndrome.
    Sofer S; Bar-Ziv J; Abeliovich D
    Am J Med Genet; 1983 Jan; 14(1):151-7. PubMed ID: 6829604
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Microtia and meatal atresia in mother and son.
    Guizar-Vázquez J; Arredondo-Vega F; Rostenberg I; Manzano C; Armendares S
    Clin Genet; 1978 Aug; 14(2):80-2. PubMed ID: 688691
    [No Abstract]   [Full Text] [Related]  

  • 60. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
    Abu-Libdeh B; Fujimoto A; Ehinger M
    Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.