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 *

99 related articles for article (PubMed ID: 8851768)

  • 1. Malpuech facial clefting syndrome in a Japanese boy with cardiac defects.
    Chinen Y; Naritomi K
    Jpn J Hum Genet; 1995 Dec; 40(4):335-8. PubMed ID: 8851768
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Apparent Malpuech syndrome: report on three Brazilian patients with additional signs.
    Guion-Almeida ML
    Am J Med Genet; 1995 Jul; 58(1):13-7. PubMed ID: 7573149
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Apparently new MCA/MR syndrome in sibs with cleft lip and palate and other facial, eye, heart, and intestinal anomalies.
    Kapur S; Toriello HV
    Am J Med Genet; 1991 Dec; 41(4):423-5. PubMed ID: 1776630
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A 580 kb microdeletion in 17q21.32 associated with mental retardation, microcephaly, cleft palate, and cardiac malformation.
    Rooryck C; Burgelin I; Stef M; Taine L; Thambo JB; Lacombe D; Arveiler B
    Eur J Med Genet; 2008; 51(1):74-80. PubMed ID: 18024240
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Syndrome of mental retardation, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, growth failure and craniosynostosis.
    Lowry RB; MacLean JR
    Birth Defects Orig Artic Ser; 1977; 13(3B):203-28. PubMed ID: 890093
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia: confirmation of the ROCA-Wiedemann syndrome.
    Zampino G; Balducci F; Mariotti P; Dickmann A; Mastroiacovo P
    Am J Med Genet; 2000 Feb; 90(5):358-60. PubMed ID: 10706355
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Malpuech syndrome: broadening the clinical spectrum and molecular analysis by array-CGH.
    Priolo M; Ciccone R; Bova I; Campolo G; Laganà C; Zuffardi O
    Eur J Med Genet; 2007; 50(2):139-43. PubMed ID: 17140870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Schinzel-Giedion syndrome].
    Okamoto N
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):35-7. PubMed ID: 11057134
    [No Abstract]   [Full Text] [Related]  

  • 11. Opitz (BBB/G) syndrome: oral manifestations.
    Brooks JK; Leonard CO; Coccaro PJ
    Am J Med Genet; 1992 Jun; 43(3):595-601. PubMed ID: 1605255
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
    Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Malpuech syndrome: a possible relationship with the Wolf-Hirschhorn/Pitt-Roger-Danks phenotype.
    Selicorni A; Faravelli F
    Am J Med Genet; 2000 Nov; 95(3):291. PubMed ID: 11102941
    [No Abstract]   [Full Text] [Related]  

  • 14. First report of glaucoma as a feature of the 3C syndrome.
    Saraiva JM; Gama E; Pires MM; Sequeira JF
    Clin Dysmorphol; 1995 Apr; 4(2):156-60. PubMed ID: 7606323
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E; Clemens M
    Am J Med Genet; 1996 Mar; 62(1):58-60. PubMed ID: 8779326
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndrome.
    Reynolds JF; Neri G; Herrmann JP; Blumberg B; Coldwell JG; Miles PV; Opitz JM
    Am J Med Genet; 1986 Nov; 25(3):413-27. PubMed ID: 3789005
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cardio-facio-cutaneous (CFC) syndrome: report of a new patient.
    Chrzanowska K; Fryns JP; Van den Berghe H
    Am J Med Genet; 1989 Aug; 33(4):471-3. PubMed ID: 2596505
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
    Casaccia G; Mobili L; Braguglia A; Santoro F; Bagolan P
    Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Carpenter's syndrome].
    Piussan C; Van Poperinghe M; Grumbach Y; Audebert M; Helsemans C; Risbourg B
    Arch Fr Pediatr; 1977 Nov; 34(9):891-8. PubMed ID: 606189
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.
    Curry CJ; Carey JC; Holland JS; Chopra D; Fineman R; Golabi M; Sherman S; Pagon RA; Allanson J; Shulman S
    Am J Med Genet; 1987 Jan; 26(1):45-57. PubMed ID: 3812577
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.