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 *

114 related articles for article (PubMed ID: 3276203)

  • 41. MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome.
    Happle R; Daniëls O; Koopman RJ
    Am J Med Genet; 1993 Oct; 47(5):710-3. PubMed ID: 8267001
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Microcephaly, microphthalmia, falciform retinal folds, and blindness. A new syndrome.
    Jarmas AL; Weaver DD; Ellis FD; Davis A
    Am J Dis Child; 1981 Oct; 135(10):930-3. PubMed ID: 7293993
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Microphthalmia, marked short stature, hearing loss, and developmental delay: extension of the phenotype of GOMBO syndrome?
    Farrell SA
    Am J Med Genet; 1997 Oct; 72(1):18-23. PubMed ID: 9295068
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. An/micr-ophthalmia, cleft lip/palate, and short limbs: a new syndrome simulating a short rib syndrome.
    Kariminejad A; Ghaderi-Sohi S; Kariminejad MH; Lachman R
    Fetal Pediatr Pathol; 2012 Oct; 31(5):295-9. PubMed ID: 22432872
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Anorectal anomalies, diaphragmatic defect, cleft palate, lower lip pits, hypopigmentation and hypogammaglobulinemia A in Kabuki syndrome: a rare combination.
    Abdel-Salam GM; Afifi HH; Eid MM; el-Badry TH; Kholoussi NM
    Genet Couns; 2008; 19(3):309-17. PubMed ID: 18990987
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The Nance-Horan syndrome.
    Walpole IR; Hockey A; Nicoll A
    J Med Genet; 1990 Oct; 27(10):632-4. PubMed ID: 2246772
    [No Abstract]   [Full Text] [Related]  

  • 48. A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformations.
    Rutledge JC; Friedman JM; Harrod MJ; Currarino G; Wright CG; Pinckney L; Chen H
    Am J Med Genet; 1984 Oct; 19(2):255-64. PubMed ID: 6507477
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy?
    Bird LM; Krous HF; Eichenfield LF; Swalwell CI; Jones MC
    Am J Med Genet; 1994 Nov; 53(2):141-8. PubMed ID: 7856638
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review.
    Gambrelle J; Till M; Lukusa B; Beby F; Mory N; Sann L; Kodjikian L; Grange JD; Putet G
    Ophthalmic Genet; 2007 Jun; 28(2):105-9. PubMed ID: 17558854
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Bilateral extreme microphthalmos.
    Guyer DR; Green WR
    Ophthalmic Paediatr Genet; 1984 Aug; 4(2):81-90. PubMed ID: 6085839
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: association or new syndrome?
    Pavone P; Parano E; Polizzi A; Trifiletti RR
    Am J Med Genet; 2000 Jun; 92(4):278-80. PubMed ID: 10842296
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A new case of Balci's syndrome (corneal opacity, microphthalmia, microcephaly, mental retardation, and generalized muscular spasticity associated with congenital heart disease).
    Balci S; Demirçeken FG; Ocal B; Zorlu P; Teziç T
    Turk J Pediatr; 2001; 43(4):366-8. PubMed ID: 11765173
    [TBL] [Abstract][Full Text] [Related]  

  • 54. X-linked syndrome of branchial arch and other defects.
    Toriello HV; Higgins JV; Abrahamson J; Waterman DF; Moore WD
    Am J Med Genet; 1985 May; 21(1):137-42. PubMed ID: 4039890
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Delineation of EFTUD2 haploinsufficiency-related phenotypes through a series of 36 patients.
    Lehalle D; Gordon CT; Oufadem M; Goudefroye G; Boutaud L; Alessandri JL; Baena N; Baujat G; Baumann C; Boute-Benejean O; Caumes R; Decaestecker C; Gaillard D; Goldenberg A; Gonzales M; Holder-Espinasse M; Jacquemont ML; Lacombe D; Manouvrier-Hanu S; Marlin S; Mathieu-Dramard M; Morin G; Pasquier L; Petit F; Rio M; Smigiel R; Thauvin-Robinet C; Vasiljevic A; Verloes A; Malan V; Munnich A; de Pontual L; Vekemans M; Lyonnet S; Attié-Bitach T; Amiel J
    Hum Mutat; 2014 Apr; 35(4):478-85. PubMed ID: 24470203
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Autopsy case of multiple anomalies with hypoplastic cerebrum, eyes, and endocrine organs, mimicking Micro syndrome.
    Hamano K; Kumada S; Nagata J; Kurata K; Hayashi M; Kojima H
    J Child Neurol; 2003 Jan; 18(1):54-7. PubMed ID: 12661939
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Anomalies associated with cleft lip, cleft palate, or both.
    Shprintzen RJ; Siegel-Sadewitz VL; Amato J; Goldberg RB
    Am J Med Genet; 1985 Apr; 20(4):585-95. PubMed ID: 3993684
    [TBL] [Abstract][Full Text] [Related]  

  • 58. De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies.
    Temple IK; Hurst JA; Hing S; Butler L; Baraitser M
    J Med Genet; 1990 Jan; 27(1):56-8. PubMed ID: 2308156
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Syndromic ear anomalies and renal ultrasounds.
    Wang RY; Earl DL; Ruder RO; Graham JM
    Pediatrics; 2001 Aug; 108(2):E32. PubMed ID: 11483842
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Ocular findings in a new heritable syndrome of brain, eye, and urogenital abnormalities.
    Duker JS; Weiss JS; Siber M; Bieber FR; Albert DM
    Am J Ophthalmol; 1985 Jan; 99(1):51-5. PubMed ID: 3917610
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.