BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 2063891)

  • 1. Trigonobrachycephaly, bulbous bifid nose, macrostomia, micrognathia, acral anomalies, and hypotonia in sibs.
    Teebi AS
    Am J Med Genet; 1991 Mar; 38(4):529-31. PubMed ID: 2063891
    [No Abstract]   [Full Text] [Related]  

  • 2. Costello syndrome: the natural history of a true postnatal growth retardation syndrome.
    Umans S; Decock P; Fryns JP
    Genet Couns; 1995; 6(2):121-5. PubMed ID: 7546454
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.
    Zwamborn-Hanssen AM; Schrander-Stumpel CT; Smeets E; Decock P; Fryns JP
    Genet Couns; 1995; 6(4):313-9. PubMed ID: 8775418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Distinct familial syndrome of severe to profound mental retardation, spastic paraplegia with contrasting axial hypotonia, short stature and distinct craniofacial appearance with nasal hypoplasia.
    Fryns JP; Devriendt K; Detroch C; Decock P
    Genet Couns; 1998; 9(1):51-4. PubMed ID: 9555588
    [No Abstract]   [Full Text] [Related]  

  • 5. Hypospadias as a new congenital anomaly in Bowen-Conradi syndrome.
    Aynaci FM; Mocan H; Erduran E; Gedik Y
    Genet Couns; 1994; 5(4):369-71. PubMed ID: 7888139
    [No Abstract]   [Full Text] [Related]  

  • 6. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation.
    Mathieu M; De Broca A; Bony H; Piussan C
    Genet Couns; 1993; 4(4):299-303. PubMed ID: 8110419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
    Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo interstitial deletion q16.2q21 on chromosome 6.
    Villa A; Urioste M; Bofarull JM; Martínez-Frías ML
    Am J Med Genet; 1995 Jan; 55(3):379-83. PubMed ID: 7726240
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
    Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
    Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FG syndrome in a premature male.
    Bianchi DW
    Am J Med Genet; 1984 Oct; 19(2):383-6. PubMed ID: 6507484
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dominant inheritance of bifid nose.
    Anyane-Yeboa K; Raifman MA; Berant M; Frogel MP; Travers H
    Am J Med Genet; 1984 Mar; 17(3):561-3. PubMed ID: 6711607
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 2q35qter duplication syndrome: phenotypic definition.
    Grammatico P; Di Rosa C; Rinaldi R; Roccella M; Cupilari F; Sbezzi T; Del Porto G
    Genet Couns; 1997; 8(4):327-34. PubMed ID: 9457503
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Polyhydramnios and paroxysmal atrial tachycardia as first clinical signs in Costello syndrome.
    Fryns JP; Devlieger H; Gewillig M; Lukusa P; Devriendt K
    Genet Couns; 1996; 7(3):237-9. PubMed ID: 8897048
    [No Abstract]   [Full Text] [Related]  

  • 14. Craniofrontonasal dysplasia: more severe expression in the mother than in her son.
    Devriendt K; Van Mol C; Fryns JP
    Genet Couns; 1995; 6(4):361-4. PubMed ID: 8775424
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The G syndrome: description of a case/and familial studies].
    Calandi C; Adami-Lami Conti C; Mannini A; Fantacci C; Nistri R; Giovannucci ML
    Arch De Vecchi Anat Patol; 1980; 64(1):59-73. PubMed ID: 7027970
    [No Abstract]   [Full Text] [Related]  

  • 16. Teschler-Nicola/Killian syndrome.
    Pagon RA
    J Clin Dysmorphol; 1983; 1(3):18-9. PubMed ID: 6584556
    [No Abstract]   [Full Text] [Related]  

  • 17. German syndrome in sibs.
    Lewin SO; Hughes HE
    Am J Med Genet; 1987 Feb; 26(2):385-90. PubMed ID: 3812590
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL; Venter PA; Du Toit JL; Shipalana N; Gericke GS
    Am J Med Genet; 1994 Jun; 51(2):98-101. PubMed ID: 8092201
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New syndrome in three affected siblings.
    Crane JP; Heise RL
    Pediatrics; 1981 Aug; 68(2):235-7. PubMed ID: 7267231
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
    Young RS; Weaver DD; Kukolich MK; Heerema NA; Palmer CG; Kawira EL; Bender HA
    Am J Med Genet; 1984 Feb; 17(2):437-50. PubMed ID: 6199974
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.