BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 5085485)

  • 1. Acrocephalopolysyndactyly, type II (Carpenter syndrome).
    Der Kaloustian VM; Sinno AA; Nassar SI
    Am J Dis Child; 1972 Nov; 124(5):716-8. PubMed ID: 5085485
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D; Farriaux JP
    J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131
    [No Abstract]   [Full Text] [Related]  

  • 4. Carpenter's syndrome. Report of a case.
    Saxena S; Sharma JC; Garg OP
    Indian J Pediatr; 1970 Dec; 37(275):627-8. PubMed ID: 5515253
    [No Abstract]   [Full Text] [Related]  

  • 5. [Laurence-Moon-Bardet-Biedl disease. A clinical contribution (author's transl)].
    Lovisetto P; Biarese V; Trenta N; Rizzi G
    Ann Endocrinol (Paris); 1974; 35(5):547-61. PubMed ID: 4377073
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. Acrocephalopolysyndactyly, type Noack, in a large kindred.
    Robinow M; Sorauf TJ
    Birth Defects Orig Artic Ser; 1975; 11(5):99-106. PubMed ID: 1240778
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies.
    Klein D; Ammann F
    J Neurol Sci; 1969; 9(3):479-513. PubMed ID: 5367041
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Carpenter syndrome in a patient from Tanzania.
    Lodhia J; Rego-Garcia I; Koipapi S; Sadiq A; Msuya D; Spaendonk RV; Hamel B; Dekker M
    Am J Med Genet A; 2021 Mar; 185(3):986-989. PubMed ID: 33368989
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes.
    Robin NH; Segel B; Carpenter G; Muenke M
    Am J Med Genet; 1996 Mar; 62(2):184-91. PubMed ID: 8882401
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Skeletal anomalies in genetically determined congenital heart disease.
    Poznanski AK; Stern AM; Gall JC
    Radiol Clin North Am; 1971 Dec; 9(3):435-58. PubMed ID: 5145748
    [No Abstract]   [Full Text] [Related]  

  • 13. Lethal short-rib polydactyly syndrome of the Majewski type: a report of three cases.
    Cooper CP; Hall CM
    Radiology; 1982 Aug; 144(3):513-7. PubMed ID: 7100463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Carpenter's syndrome in an 11-year-old girl].
    Bartkowiak K; Piontek E; Pawlaczyk B
    Pediatr Pol; 1972; 47(3):349-51. PubMed ID: 5019700
    [No Abstract]   [Full Text] [Related]  

  • 15. Laurence-Moon syndrome: evaluation of endocrinological function and phenotypic concordance and report of cases.
    Dekaban AS; Parks JS; Ross GT
    Med Ann Dist Columbia; 1972 Nov; 41(11):687-94. PubMed ID: 4508225
    [No Abstract]   [Full Text] [Related]  

  • 16. The Laurence-Moon-Bardet-Biedl-syndrome.
    Luz MF; Marques MN; Jorge E; Jacomini CZ; Ribero Z; Marques J
    Metab Pediatr Syst Ophthalmol (1985); 1985; 8(2-3):15-20. PubMed ID: 3870940
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cerebral malformations in Carpenter syndrome.
    Taravath S; Tonsgard JH
    Pediatr Neurol; 1993; 9(3):230-4. PubMed ID: 8352858
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Polydactylia].
    Duca-Marinescu D; Maximilian C
    Rev Pediatr Obstet Ginecol Pediatr; 1975; 24(1):89-93. PubMed ID: 810850
    [No Abstract]   [Full Text] [Related]  

  • 19. Acrocallosal syndrome: a new case.
    Lungarotti MS; Marinelli D; Mezzetti D; Caputo N; Calabro A
    Am J Med Genet; 1991 Jul; 40(1):94-6. PubMed ID: 1887856
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tricho-rhino-phalangeal syndrome type III.
    Kajii T; Fernandez Gonzalez I; Matsuura S
    Am J Med Genet; 1994 Feb; 49(3):349-50. PubMed ID: 8209900
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.