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 *

1113 related articles for article (PubMed ID: 8775417)

  • 21. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G; Demeocq F; Palcoux JB; Vanlieferinghen P
    Am J Med Genet; 1983 Dec; 16(4):475-80. PubMed ID: 6660246
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome.
    Rodini ES; Richieri-Costa A
    Am J Med Genet; 1990 Aug; 36(4):473-6. PubMed ID: 2167611
    [TBL] [Abstract][Full Text] [Related]  

  • 23. "Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred.
    Jackson CE; Weiss L; Watson JH
    Pediatrics; 1974 Aug; 54(2):201-7. PubMed ID: 4847854
    [No Abstract]   [Full Text] [Related]  

  • 24. Fountain syndrome: further delineation of the clinical syndrome and follow-up data.
    Van Buggenhout GJ; Van Ravenswaaij-Arts CM; Renier WO; Van de Wiel MP; Trommelen JC; Pijkels E; Hamel BC; Fryns JP
    Genet Couns; 1996; 7(3):177-86. PubMed ID: 8897038
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [The hand-foot-uterus syndrome. A report of a case with recessive autosomal inheritance].
    Stella NC; Triolo O; Corrado F
    Minerva Ginecol; 1993 Sep; 45(9):429-32. PubMed ID: 8255504
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Roberts syndrome or "X-linked amelia"?
    Gershoni-Baruch R; Drugan A; Bronshtein M; Zimmer EZ
    Am J Med Genet; 1990 Dec; 37(4):569-72. PubMed ID: 2260610
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?
    Kotzot D; Richter K; Gierth-Fiebig K
    Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects.
    Zlotogora J; Glick B
    Am J Med Genet; 1993 Aug; 47(1):89-90. PubMed ID: 8368260
    [TBL] [Abstract][Full Text] [Related]  

  • 29. New syndromes of mental retardation.
    Thurmon TF; Santos CL
    Birth Defects Orig Artic Ser; 1975; 11(2):264-8. PubMed ID: 1227531
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Filippi syndrome: report of three additional cases.
    Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
    Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B; Hersh JH
    Am J Med Genet; 1997 Aug; 71(2):211-4. PubMed ID: 9217224
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The 18p- syndrome. Report of five cases.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A; Pereira SC
    Am J Med Genet; 1992 Mar; 42(5):681-7. PubMed ID: 1632438
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.
    Pena SD; Shokeir MH
    Birth Defects Orig Artic Ser; 1976; 12(5):201-8. PubMed ID: 953225
    [No Abstract]   [Full Text] [Related]  

  • 35. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
    Børglum AD; Balslev T; Haagerup A; Birkebaek N; Binderup H; Kruse TA; Hertz JM
    Eur J Hum Genet; 2001 Oct; 9(10):753-7. PubMed ID: 11781686
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dysmorphology report holoprosencephaly-polydactyly syndrome: affected brother and sister with a wide spectrum of anomalies.
    Delozier-Blanchet CD; Engel E
    Genet Couns; 1992; 3(1):57-8. PubMed ID: 1590983
    [No Abstract]   [Full Text] [Related]  

  • 38. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G; Centa A; Pozzolo S; Camera A
    Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Autosomal recessive type of whistling face syndrome in twins.
    Kousseff BG; McConnachie P; Hadro TA
    Pediatrics; 1982 Mar; 69(3):328-31. PubMed ID: 7199706
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 56.