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 *

359 related articles for article (PubMed ID: 9852671)

  • 1. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M; Sugio Y
    J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
    Feingold M; Hall BD; Lacassie Y; Martínez-Frías ML
    Am J Med Genet; 1997 Mar; 69(3):245-9. PubMed ID: 9096752
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Brief clinical report: an X-linked mental retardation syndrome with craniofacial abnormalities, microcephaly and club foot.
    Holmes LB; Gang DL
    Am J Med Genet; 1984 Jan; 17(1):375-82. PubMed ID: 6711605
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H; Kishino T; Niikawa N
    Am J Med Genet; 1990 May; 36(1):89-93. PubMed ID: 2333912
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant microcephaly with mental retardation.
    Bawle E; Horton M
    Am J Med Genet; 1989 Jul; 33(3):382-4. PubMed ID: 2801773
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
    Martínez-Frías ML; Martín M; Pardo M; Fernandez de las Heras F; Frías JL
    Am J Med Genet; 1995 Jan; 55(2):213-6. PubMed ID: 7717420
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new X-linked multiple congenital anomalies/mental retardation syndrome.
    Golabi M; Ito M; Hall BD
    Am J Med Genet; 1984 Jan; 17(1):367-74. PubMed ID: 6711604
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The syndrome of Hirschsprung disease, microcephaly, unusual face, and mental retardation.
    Halal F; Morel J
    Am J Med Genet; 1990 Sep; 37(1):106-8. PubMed ID: 2240026
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Borjeson-Forssman-Lehmann syndrome. A family study.
    Dereymaeker AM; Fryns JP; Hoefnagels M; Heremans G; Marien J; van den Berghe H
    Clin Genet; 1986 Apr; 29(4):317-20. PubMed ID: 3720009
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome.
    Verloes A; Lesenfants S; Philippet B; Iyawa A; Laloux F; Koulischer L
    Genet Couns; 1996; 7(4):277-82. PubMed ID: 8985731
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.
    Chudley AE; Lowry RB; Hoar DI
    Am J Med Genet; 1988 Dec; 31(4):741-51. PubMed ID: 3239563
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC; Mariman EC; van Beersum SE; Schoonbrood-Lenssen AM; Ropers HH
    Am J Med Genet; 1994 Jul; 51(4):591-7. PubMed ID: 7943045
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.
    Verloes A; Dodinval P; Beco L; Bonnivert J; Lambotte C
    Am J Med Genet; 1990 Sep; 37(1):119-23. PubMed ID: 2240028
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: possible new syndrome.
    Seemanová E; Lesný I
    Am J Med Genet; 1996 Dec; 66(2):179-83. PubMed ID: 8958326
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency.
    Weaver DD; Williams CP
    Birth Defects Orig Artic Ser; 1977; 13(3B):69-84. PubMed ID: 890101
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ruvalcaba syndrome: autosomal dominant inheritance.
    Sugio Y; Kajii T
    Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
    Bottani A; Schinzel A
    Clin Dysmorphol; 1993 Jul; 2(3):225-31. PubMed ID: 8287184
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
    Bibas Bonet H; Fontenla M; Fauze R; G de Pinat I
    Rev Neurol; 2001 Apr 16-30; 32(8):746-50. PubMed ID: 11391511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second family.
    Wulfsberg EA; Campbell AB; Lurie IW; Eanet KR
    Am J Med Genet; 1996 Jun; 63(4):554-7. PubMed ID: 8826434
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.