BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

340 related articles for article (PubMed ID: 8985482)

  • 1. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS; Kaurah P
    Am J Med Genet; 1996 Dec; 66(3):257-60. PubMed ID: 8985482
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorder.
    Seemanová E; Passarge E; Beneskova D; Houstĕk J; Kasal P; Sevcíková M
    Am J Med Genet; 1985 Apr; 20(4):639-48. PubMed ID: 3857858
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal recessive nonsyndromal microcephaly with normal intelligence.
    Teebi AS; Al-Awadi SA; White AG
    Am J Med Genet; 1987 Feb; 26(2):355-9. PubMed ID: 3812587
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A; Pereira SC
    Am J Med Genet; 1992 Mar; 42(5):681-7. PubMed ID: 1632438
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H; Kishino T; Niikawa N
    Am J Med Genet; 1990 May; 36(1):89-93. PubMed ID: 2333912
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pilodentoungulardysplasia with microcephaly: a new ectodermal dysplasia/malformation syndrome.
    Tajara EH; Pinheiro M; Freire-Maia N
    Am J Med Genet; 1987 Jan; 26(1):153-6. PubMed ID: 3812555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities.
    Woods CG; Crouchman M; Huson SM
    J Med Genet; 1992 Jul; 29(7):500-2. PubMed ID: 1640433
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
    Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E; Goecke T; Meinecke P
    Am J Med Genet; 1996 May; 63(1):185-9. PubMed ID: 8723107
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal recessive Silver-Russell syndrome.
    Teebi AS
    Clin Dysmorphol; 1992 Jul; 1(3):151-6. PubMed ID: 1285272
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Anonychia associated with ectrodactyly syndrome: a case report.
    Patiroğlu T; Hasanoğlu E
    Turk J Pediatr; 1989; 31(3):249-52. PubMed ID: 2485992
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence.
    Leung AK
    Am J Med Genet; 1987 Jan; 26(1):231. PubMed ID: 3812569
    [No Abstract]   [Full Text] [Related]  

  • 16. Autosomal recessive cleft lip/palate, ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family.
    Richieri-Costa A; Guion-Almeida ML; Freire-Maia N; Pinheiro M
    Am J Med Genet; 1992 Sep; 44(2):158-62. PubMed ID: 1456284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A; Gollop TR; Otto PG
    Am J Med Genet; 1983 Apr; 14(4):607-15. PubMed ID: 6846395
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
    Janssen HC; Schaap C; Vandevijver N; Moerman P; de Die-Smulders CE; Fryns JP
    J Med Genet; 1999 Jun; 36(6):481-4. PubMed ID: 10874639
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defects.
    Gillessen-Kaesbach G; Meinecke P; Garrett C; Padberg BC; Rehder H; Passarge E
    Am J Med Genet; 1993 Feb; 45(4):511-8. PubMed ID: 8465860
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fuhrmann syndrome of right-angle bowed femora, absence of fibulae and digital anomalies: two further cases.
    Lipson AH; Kozlowski K; Barylak A; Marsden W
    Am J Med Genet; 1991 Nov; 41(2):176-9. PubMed ID: 1785629
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.