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 *

248 related articles for article (PubMed ID: 8723070)

  • 1. Anophthalmia-Waardenburg syndrome: a report of three cases.
    Suyugül Z; Seven M; Hacihanefioğlu S; Kartal A; Suyugül N; Cenani A
    Am J Med Genet; 1996 Apr; 62(4):391-7. PubMed ID: 8723070
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Waardenburg anophthalmia syndrome: report and review.
    Cogulu O; Ozkinay F; Gündüz C; Sapmaz G; Ozkinay C
    Am J Med Genet; 2000 Jan; 90(2):173-4. PubMed ID: 10607960
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.
    Lin HJ; Kakkis ED; Eteson DJ; Lachman RS
    Am J Med Genet; 1993 Sep; 47(4):534-9. PubMed ID: 8256819
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ophthalmo-acromelic syndrome: report and review.
    Tekin M; Tutar E; Arsan S; Atay G; Bodurtha J
    Am J Med Genet; 2000 Jan; 90(2):150-4. PubMed ID: 10607955
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Anophthalmos-syndactyly (Waardenburg) syndrome without oligodactyly of toes.
    Sayli BS; Akarsu AN; Altan S
    Am J Med Genet; 1995 Jul; 58(1):18-20. PubMed ID: 7573150
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Acrodysostosis: autosomal dominant transmission.
    Sheela SR; Perti A; Thomas G
    Indian Pediatr; 2005 Aug; 42(8):822-6. PubMed ID: 16141486
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hunter-McAlpine syndrome: report of a third family.
    Adès LC; Morris LL; Simpson DA; Haan EA
    Clin Dysmorphol; 1993 Apr; 2(2):123-30. PubMed ID: 8281273
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Upper limb involvement in the Klein-Waardenburg syndrome.
    Goodman RM; Lewithal I; Solomon A; Klein D
    Am J Med Genet; 1982 Apr; 11(4):425-33. PubMed ID: 7091186
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
    Meinecke P
    Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tibial hemimelia: report on 37 new cases, clinical and genetic considerations.
    Richieri-Costa A; Ferrareto I; Masiero D; da Silva CR
    Am J Med Genet; 1987 Aug; 27(4):867-84. PubMed ID: 3425598
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.
    Nevin NC; Thomas PS; Eedy DJ; Shepherd C
    J Med Genet; 1995 Aug; 32(8):638-41. PubMed ID: 7473658
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Waardenburg's recessive anophthalmia syndrome.
    Traboulsi EI; Nasr AM; Fahd SD; Jabbour NM; Der Kaloustian VM
    Ophthalmic Paediatr Genet; 1984 Apr; 4(1):13-8. PubMed ID: 6549566
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal dominant inheritance of tetramelic monodactyly.
    Sommer A; Hines SJ
    Am J Med Genet; 1992 Jan; 42(1):51-4. PubMed ID: 1308366
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A syndrome with true anophthalmia, hand-foot defects and mental retardation.
    Pallotta R; Dallapiccola B
    Ophthalmic Paediatr Genet; 1984 Apr; 4(1):19-23. PubMed ID: 6544388
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
    Fabbro MA; D'Agostino S; Costa L; Musi L; Cappellari F
    Pediatr Med Chir; 1997; 19(2):121-4. PubMed ID: 9312747
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel homozygous variant in the SMOC1 gene underlying Waardenburg anophthalmia syndrome.
    Ullah A; Umair M; Ahmad F; Muhammad D; Basit S; Ahmad W
    Ophthalmic Genet; 2017; 38(4):335-339. PubMed ID: 28085523
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Anomalous inheritance in a kindred with split hand, split foot malformation.
    Spranger M; Schapera J
    Eur J Pediatr; 1988 Feb; 147(2):202-5. PubMed ID: 3366140
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hand-foot-genital syndrome: the importance of hallux varus.
    Cleveland RH; Holmes LB
    Pediatr Radiol; 1990; 20(5):339-43. PubMed ID: 2349017
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cooks syndrome: a case report and brief review.
    Brennan CB; Buehler T; Lesher JL
    Pediatr Dermatol; 2013; 30(4):e52-3. PubMed ID: 22329539
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.