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 *

134 related articles for article (PubMed ID: 11343342)

  • 1. New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay.
    Bacha F; Hoo JJ
    Am J Med Genet; 2001 Jun; 101(1):70-3. PubMed ID: 11343342
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cleft lip and palate, pili torti, malformed ears, partial syndactyly of fingers and toes, and mental retardation: a new syndrome?
    Zlotogora J; Zilberman Y; Tenenbaum A; Wexler MR
    J Med Genet; 1987 May; 24(5):291-3. PubMed ID: 3035184
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Micrognathia, polydactyly, and cleft palate.
    Lowry RB; Miller JR; MacLean JR
    J Pediatr; 1968 Jun; 72(6):859-61. PubMed ID: 5652614
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. The Coffin-Siris syndrome.
    Schinzel A
    Acta Paediatr Scand; 1979 May; 68(3):449-52. PubMed ID: 155976
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ectrodactyly, ectodermal dysplasia and cleft palate (EEC syndrome). Report of a family and review of the literature.
    Rosenmann A; Shapira T; Cohen MM
    Clin Genet; 1976 Mar; 9(3):347-53. PubMed ID: 1261073
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Tricho-rhino-phalangeal syndrome. Apropos of a neonatal case].
    Romanet P; Bouron Y; Yaouanc H
    Ann Pediatr (Paris); 1985 May; 32(5):473-6. PubMed ID: 4026143
    [No Abstract]   [Full Text] [Related]  

  • 8. Tricho-rhino-phalangeal syndrome.
    Hansen DD; Shewmake SW
    Int J Dermatol; 1979 Sep; 18(7):561-4. PubMed ID: 500270
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Another family with tricho-rhino-phalangeal syndrome type III (Sugio-Kajii syndrome).
    Nagai T; Nishimura G; Kasai H; Hasegawa T; Kato R; Ohashi H; Fukushima Y
    Am J Med Genet; 1994 Feb; 49(3):278-80. PubMed ID: 8209886
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A familial tetraphocomelia syndrome involving limb deformities, cleft lip, cleft palate, and associated anomalies--a new syndrome.
    Kucheria K; Bhargava SK; Bamezai R; Bhutani P
    Hum Genet; 1976 Aug; 33(3):323-6. PubMed ID: 964992
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal dominant blepharophimosis with multiple congenital anomalies.
    Krieble BF; Bixler D
    J Clin Dysmorphol; 1984; 2(1):24-9. PubMed ID: 6587013
    [No Abstract]   [Full Text] [Related]  

  • 12. Sensorineural hearing loss, small facial features, submucous cleft palate, and myoclonic seizures.
    Preus M; Cooper AR; O'Leary E
    J Clin Dysmorphol; 1984; 2(1):30-1. PubMed ID: 6587014
    [No Abstract]   [Full Text] [Related]  

  • 13. Tricho-rhino-phalangeal syndrome. Report of a family with 3 affected members.
    Voigtländer V; Osswald F
    Dermatologica; 1978; 156(1):34-9. PubMed ID: 618760
    [No Abstract]   [Full Text] [Related]  

  • 14. Robin sequence and oligodactyly in mother and son.
    Robinow M; Johnson GF; Apesos J
    Am J Med Genet; 1986 Oct; 25(2):293-7. PubMed ID: 3777025
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance.
    Meinecke P; Fryns JP
    Clin Genet; 1985 Dec; 28(6):516-20. PubMed ID: 4075561
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The oral manifestations of 4p- syndrome.
    Morishita M; Shiba R; Chiyo H; Furuyama J; Fujita H; Atsumi Y
    J Oral Maxillofac Surg; 1983 Sep; 41(9):601-5. PubMed ID: 6577152
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Contribution to the genetics of the orofaciodigital syndrome].
    Stahl A; Fuhrmann W; Schroeder TM
    Fortschr Kieferorthop; 1965; 26(4):455-64. PubMed ID: 5328904
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Cleidocranial dysostosis, severe micrognathism, bilateral absence of thumbs and first metatarsal bone, and distal aphalangia: a new genetic syndrome.
    Yunis E; Varón H
    Am J Dis Child; 1980 Jul; 134(7):649-53. PubMed ID: 7395825
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cleft-palate lateral synechia syndrome: insight into the phenotypic spectrum of Fryns syndrome?
    Jaeger A; Kapur R; Whelan M; Leung E; Cunningham M
    Birth Defects Res A Clin Mol Teratol; 2003 Jun; 67(6):460-6. PubMed ID: 12962292
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.