These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 4708024)

  • 1. A new syndrome of broad terminal phalanges and facial abnormalities.
    Keipert JA; Fitzgerald MG; Danks DM
    Aust Paediatr J; 1973 Feb; 9(1):10-3. PubMed ID: 4708024
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. Familial broad terminal phalanges with one individual showing additional anomalies.
    Pavone L; Sorge G; Pavone V; Rizzo R; Ruggieri M; Polizzi A; Opitz JM
    Am J Med Genet; 1997 Aug; 71(3):271-4. PubMed ID: 9268094
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The Coffin-Siris syndrome. A new syndrome of mental retardation, hypo-aplasia of the nails and terminal phalanges of the 5th fingers and toes].
    Mastroiacovo P; Salvaggio E; Parenti D
    Minerva Pediatr; 1977 Mar; 29(11):773-8. PubMed ID: 875947
    [No Abstract]   [Full Text] [Related]  

  • 5. Choanal atresia in two unrelated patients with the Coffin-Siris syndrome.
    de Jong G; Nelson MM
    Clin Genet; 1992 Dec; 42(6):320-2. PubMed ID: 1493645
    [No Abstract]   [Full Text] [Related]  

  • 6. Postaxial acrofacial dysostosis or Miller syndrome. A case report.
    Barbuti D; Orazi C; Reale A; Paradisi C
    Eur J Pediatr; 1989 Feb; 148(5):445-6. PubMed ID: 2920751
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The dermatoglyphics of the 18q- syndrome.
    Mavalwala J; Wilson MG; Parker CE
    Am J Phys Anthropol; 1970 May; 32(3):443-9. PubMed ID: 5419379
    [No Abstract]   [Full Text] [Related]  

  • 8. [Rubinstein-Taybi syndrome of broad thumbs and broad big toes with cranio-mandibulo-facial malformations and mental retardation].
    Weiland R
    Arch Kinderheilkd; 1969 May; 179(1):78-90. PubMed ID: 5799636
    [No Abstract]   [Full Text] [Related]  

  • 9. Six patients with oral-facial-digital syndrome IV: the case for heterogeneity.
    Toriello HV; Carey JC; Suslak E; Desposito FR; Leonard B; Lipson M; Friedman BD; Hoyme HE
    Am J Med Genet; 1997 Mar; 69(3):250-60. PubMed ID: 9096753
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mental retardation with facial abnormalities, broad thumbs and toes and unusual dermatoglyphics.
    Davison BC; Ellis HL; Kuzemko JA; Roberts DF
    Dev Med Child Neurol; 1967 Oct; 9(5):588-93. PubMed ID: 5587707
    [No Abstract]   [Full Text] [Related]  

  • 11. Extending the Pallister-Hall syndrome to include other central nervous system malformations.
    Finnigan DP; Clarren SK; Haas JE
    Am J Med Genet; 1991 Sep; 40(4):395-400. PubMed ID: 1746599
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A patient with facial abnormality, imperforate anus, tetrapolyhypodactyly and meningocele: a variable manifestation of the polyoligodactyly/imperforate anus/vertebral anomalies syndrome.
    Sener RN
    Pediatr Radiol; 1994; 24(8):598-9. PubMed ID: 7724288
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Marchesani syndrome.
    Amla I; Krishna GS; Mruthyunijaya GT
    J Indian Med Assoc; 1972 Dec; 59(12):517-20. PubMed ID: 4658301
    [No Abstract]   [Full Text] [Related]  

  • 14. Unusual type of brachydactyly associated with short stature and facial anomalies. A new syndrome?
    Richieri-Costa A; Colletto GM; Otto PA
    Am J Med Genet; 1985 Aug; 21(4):637-42. PubMed ID: 4025394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tricho-rhino-phalangeal syndrome.
    Kozlowski K; Blaim A; Malolepszy E
    Australas Radiol; 1972 Dec; 16(4):411-6. PubMed ID: 4661984
    [No Abstract]   [Full Text] [Related]  

  • 16. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis.
    Clayton-Smith J; Donnai D
    J Med Genet; 1989 May; 26(5):339-42. PubMed ID: 2732996
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Orofaciodigital syndrome. Apropos of an 11th case in the same family].
    Vissian L; Vaillaud JC
    Ann Dermatol Syphiligr (Paris); 1972; 99(1):5-20. PubMed ID: 5053179
    [No Abstract]   [Full Text] [Related]  

  • 18. Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome.
    Park SC; Needles CF; Dimich I; Sussman L
    J Pediatr; 1968 Dec; 73(6):896-902. PubMed ID: 4386913
    [No Abstract]   [Full Text] [Related]  

  • 19. Rubinstein-Taybi syndrome.
    Gellis SS; Feingold M
    Am J Dis Child; 1971 Apr; 121(4):327-8. PubMed ID: 5550739
    [No Abstract]   [Full Text] [Related]  

  • 20. The Coffin-Siris syndrome. A report of four cases and review of the literature.
    Lucaya J; Garcia-Conesa JA; Bosch-Banyeras JM; Pons-Peradejordi G
    Pediatr Radiol; 1981; 11(1):35-8. PubMed ID: 7019832
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.