BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

66 related articles for article (PubMed ID: 6863957)

  • 1. Acrocephalopolysyndactyly syndrome (type II).
    Tak SK; Mehta R; Ranka SL; Bhandari B
    J Indian Med Assoc; 1983 Feb; 80(3-4):57-8, 60. PubMed ID: 6863957
    [No Abstract]   [Full Text] [Related]  

  • 2. Acrocephalopolysyndactyly--type II. (Carpenter's syndrome) in two siblings. Case reports.
    Paul SS; Punnachalil M
    Indian Pediatr; 1979 Feb; 16(2):191-5. PubMed ID: 457235
    [No Abstract]   [Full Text] [Related]  

  • 3. Apert syndrome with omphalocele: a case report.
    Ercoli G; Bidondo MP; Senra BC; Groisman B
    Birth Defects Res A Clin Mol Teratol; 2014 Sep; 100(9):726-9. PubMed ID: 25045033
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes.
    Cohen DM; Green JG; Miller J; Gorlin RJ; Reed JA
    Am J Med Genet; 1987 Oct; 28(2):311-24. PubMed ID: 3322002
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Carpenter's syndrome (acrocephalopolysyndactyly) in two siblings].
    Svirsky-Fein S; Langer L; Tomer A; Legum C
    Harefuah; 1978 Apr; 94(7-8):231-4. PubMed ID: 669457
    [No Abstract]   [Full Text] [Related]  

  • 6. Carpenter syndrome--acrocephalopolysyndactyly type II.
    Eaton AP; Sommer A; Kontras SB; Sayers MP
    Birth Defects Orig Artic Ser; 1974; 10(9):249-60. PubMed ID: 4370930
    [No Abstract]   [Full Text] [Related]  

  • 7. Carpenter's syndrome: acrocephalopolysyndactyly. An autosomal recessive syndrome.
    Temtamy SA
    J Pediatr; 1966 Jul; 69(1):111-20. PubMed ID: 5935752
    [No Abstract]   [Full Text] [Related]  

  • 8. Familial omphalocele: analysis of risk factors and case report.
    DiLiberti JH
    Am J Med Genet; 1982 Nov; 13(3):263-8. PubMed ID: 7180872
    [No Abstract]   [Full Text] [Related]  

  • 9. Otopalatodigital syndrome type II associated with omphalocele: report of three cases.
    Young K; Barth CK; Moore C; Weaver DD
    Am J Med Genet; 1993 Feb; 45(4):481-7. PubMed ID: 8465856
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Acrocephalopolysyndactyly type IV: a new genetic syndrome in 3 sibs.
    Goodman RM; Sternberg M; Shem-Tov Y; Katznelson MB; Hertz M; Rotem Y
    Clin Genet; 1979 Mar; 15(3):209-14. PubMed ID: 421359
    [No Abstract]   [Full Text] [Related]  

  • 11. Umbilical hernia of infants and children.
    Mbanefo SE
    J R Coll Gen Pract; 1971 Feb; 21(103):92-5. PubMed ID: 5560071
    [No Abstract]   [Full Text] [Related]  

  • 12. [Acrocephalopolysyndactyly (type II (McKusick) acrocephalosyndactyly or Carpenter's syndrome. Report on 4 cases and an observation of the syndrome of Marshall-Smith (author's transl)].
    Pfeiffer RA; Seemann KB; Tünte W; Gussone J; Klemm E
    Klin Padiatr; 1977 Mar; 189(2):120-30. PubMed ID: 558466
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sliding hiatal hernia associated with Apert syndrome: a first case report.
    Tastekin A; Kantarci M; Ors R; Ceviz N
    Genet Couns; 2004; 15(3):387-9. PubMed ID: 15517835
    [No Abstract]   [Full Text] [Related]  

  • 14. Rieger syndrome with exomphalos.
    Reddihough DS; Rogers JG; Keith CG
    Aust Paediatr J; 1982 Jun; 18(2):130-1. PubMed ID: 6814412
    [No Abstract]   [Full Text] [Related]  

  • 15. [Wiedemann and Beckwith syndrome: a new familial case].
    Piussan C; Risbourg B; Lenaerts C; Delvallez N; Gontier MF; Vitse M
    J Genet Hum; 1980 Sep; 28(3):281-91. PubMed ID: 7463028
    [No Abstract]   [Full Text] [Related]  

  • 16. Acrocephalolysyndactyly type II (Carpenter's syndrome).
    Puri V; Thirupuram S; Jain TS; Khalil A; Saha MM
    Indian Pediatr; 1980 Feb; 17(2):175-7. PubMed ID: 7450848
    [No Abstract]   [Full Text] [Related]  

  • 17. Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?
    Donnai D; Barrow M
    Am J Med Genet; 1993 Oct; 47(5):679-82. PubMed ID: 8266995
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lethal multiple pterygium syndrome associated with omphalocele.
    Chen CP
    Genet Couns; 2007; 18(4):451-3. PubMed ID: 18286827
    [No Abstract]   [Full Text] [Related]  

  • 19. [The Beckwith-Wiedemann syndrome. Six observations with three familial forms (author's transl)].
    Labbe A; Demeocq F; Gaulme J; Masson A; Malpuech G
    Ann Pediatr (Paris); 1981 Nov; 28(9):665-70. PubMed ID: 7316412
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.