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 *

87 related articles for article (PubMed ID: 1162223)

  • 21. Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency.
    Ballabio A; Zollo M; Carrozzo R; Caiulo A; Zuffardi O; Cascioli CF; Viggiano D; Strisciuglio P
    Am J Med Genet; 1991 Nov; 41(2):184-7. PubMed ID: 1785631
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A family with three recessive traits and homozygosity for a long 9qh+ chromosome segment.
    Christian JC; Dexter RN; Palmer CG; Muller J
    Am J Med Genet; 1980; 6(4):301-8. PubMed ID: 6938130
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Short stature, mental retardation, eye anomalies, and cleft lip/palate.
    Richieri-Costa A; Guion-Almeida ML
    Am J Med Genet; 1992 Feb; 42(4):449-52. PubMed ID: 1609826
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency.
    Hurst JA; Baraitser M; Winter RM
    Am J Med Genet; 1987 Dec; 28(4):965-70. PubMed ID: 3688035
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Deletion of distal promoter of VCXA in a patient with X-linked ichthyosis associated with borderline mental retardation.
    Hosomi N; Oiso N; Fukai K; Hanada K; Fujita H; Ishii M
    J Dermatol Sci; 2007 Jan; 45(1):31-6. PubMed ID: 17113756
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophy.
    Stoll C; Eyer D
    Ann Genet; 1999; 42(1):45-50. PubMed ID: 10214507
    [TBL] [Abstract][Full Text] [Related]  

  • 28. An apparently new syndrome of microcephalic primordial dwarfism and cataracts.
    Toriello HV; Horton WA; Oostendorp A; Waterman DF; Higgins JV
    Am J Med Genet; 1986 Sep; 25(1):1-8. PubMed ID: 3799711
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mental retardation/shortness of stature/multiple minor anomalies syndrome associated with insertion of 3q material into 18p.
    al-Attia HM; Sedaghatian MR
    Am J Med Genet; 1995 Mar; 56(1):35-8. PubMed ID: 7747783
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Familial ichthyosis, dwarfism, mental retardation, and renal disease.
    Rayner A; Lampert RP; Rennert OM
    J Pediatr; 1978 May; 92(5):766-8. PubMed ID: 641625
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Familial and hereditary microcephaly. Study of 10 cases in 4 families].
    Bost M; Crouzet G; Jalbert P; Lesage A; Beaudoing A
    Pediatrie; 1971 Sep; 26(6):587-98. PubMed ID: 5116340
    [No Abstract]   [Full Text] [Related]  

  • 33. Familial partial duplication (1)(p21p31).
    Hoechstetter L; Soukup S; Schorry EK
    Am J Med Genet; 1995 Nov; 59(3):291-4. PubMed ID: 8599351
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes.
    Mochel F; Missirian C; Reynaud R; Moncla A
    Eur J Med Genet; 2008; 51(1):68-73. PubMed ID: 18194880
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Sjögren-Larsson syndrome. Study of 2 cases].
    Cabezuelo-Huerta G; Mulas F; Frontera-Izquierdo P
    An Esp Pediatr; 1983 May; 18(5):399-402. PubMed ID: 6614675
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter.
    Ross JB; Allderdice PW; Shapiro LJ; Aveling J; Eales BA; Simms D
    Arch Dermatol; 1985 Dec; 121(12):1524-8. PubMed ID: 3864397
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D.
    Kleijer WJ; Beemer FA; Boom BW
    Am J Med Genet; 1994 Aug; 52(2):227-30. PubMed ID: 7802014
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome.
    Soekarman D; Fryns JP
    Genet Couns; 1992; 3(2):111-3. PubMed ID: 1642808
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Type C hereditary brachydactyly. Clinical and genetic study of 3 families].
    Gnamey D; Walbaum R; Saint-Aubert P; Fontaine G
    Ann Pediatr (Paris); 1971; 18(6):438-49. PubMed ID: 5564915
    [No Abstract]   [Full Text] [Related]  

  • 40. A novel congenital ichthyosiform syndrome with associated panhypopituitarism, corneal opacities and mental retardation.
    Pandhi D; Khanna D; Singal A; Madhu SV
    Arch Dermatol Res; 2007 Nov; 299(9):457-60. PubMed ID: 17786459
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.