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 *

110 related articles for article (PubMed ID: 5567967)

  • 1. A new familial syndrome with osseous dysplasia and mental dificiency.
    Ruvalcaba RH; Reichert A; Smith DW
    J Pediatr; 1971 Sep; 79(3):450-5. PubMed ID: 5567967
    [No Abstract]   [Full Text] [Related]  

  • 2. Microcephaly, mild mental retardation, short stature, and skeletal anomalies in siblings.
    Zackai EH; Sly WS; McAlister WG
    Am J Dis Child; 1972 Jul; 124(1):111-5. PubMed ID: 5033742
    [No Abstract]   [Full Text] [Related]  

  • 3. Epiphyseal dysplasia, microcephaly, nystagmus, and retinitis pigmentosa.
    Lowry RB; Wood BJ; Cox TA; Hayden MR
    Am J Med Genet; 1989 Jul; 33(3):341-5. PubMed ID: 2801768
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus.
    Lowry B; Miller JR; Fraser FC
    Am J Dis Child; 1971 Jun; 121(6):496-500. PubMed ID: 5581017
    [No Abstract]   [Full Text] [Related]  

  • 5. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.
    Mattei JF; Collignon P; Ayme S; Giraud F
    Clin Genet; 1983 Jan; 23(1):70-4. PubMed ID: 6682021
    [No Abstract]   [Full Text] [Related]  

  • 6. X-linked skeletal dysplasia with mental retardation.
    Christian JC; DeMyer Franken EA; Huff JS; Khairi S; Reed T
    Clin Genet; 1977 Feb; 11(2):128-36. PubMed ID: 837562
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.
    Gall JC; Stern AM; Poznanski AK; Garn SM; Weinstein ED; Hayward JR
    Am J Hum Genet; 1972 Jan; 24(1):24-36. PubMed ID: 5012690
    [No Abstract]   [Full Text] [Related]  

  • 8. A new familial metabolic disorder with progressive osseous changes, microcephaly, coarse facies, flat nasal bridge and severe mental retardation.
    Hall BD; Riggs FD
    Birth Defects Orig Artic Ser; 1975; 11(5):79-90. PubMed ID: 1218240
    [No Abstract]   [Full Text] [Related]  

  • 9. Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia.
    Porteous ME; Burn J
    J Med Genet; 1990 May; 27(5):339-40. PubMed ID: 2352265
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Coffin-Lowry syndrome. A study of two new index patients and their families.
    Haspeslagh M; Fryns JP; Beusen L; Van Dessel F; Vinken L; Moens E; Van den Berghe H
    Eur J Pediatr; 1984 Dec; 143(2):82-6. PubMed ID: 6519116
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.
    Gurrieri F; Sammito V; Bellussi A; Neri G
    Am J Med Genet; 1992 Oct; 44(3):315-20. PubMed ID: 1488978
    [No Abstract]   [Full Text] [Related]  

  • 12. A familial syndrome of short stature associated with facial dysplasia and genital anomalies.
    Aarskog D
    Birth Defects Orig Artic Ser; 1971 May; 7(6):235-9. PubMed ID: 4155960
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chorio-retinal dysplasia, microcephaly and mental retardation. An autosomal dominant syndrome.
    Tenconi R; Clementi M; Moschini GB; Casara G; Baccichetti C
    Clin Genet; 1981 Nov; 20(5):347-51. PubMed ID: 7333029
    [No Abstract]   [Full Text] [Related]  

  • 14. Familial syndrome of mental retardation, short stature, contractures of the hands, and genital anomalies.
    Urban MD; Rogers JG; Meyer WJ
    J Pediatr; 1979 Jan; 94(1):52-5. PubMed ID: 758422
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hall-Riggs syndrome: a possible second affected family?
    Silengo M; Rigardetto R
    J Med Genet; 2000 Nov; 37(11):886-9. PubMed ID: 11185076
    [No Abstract]   [Full Text] [Related]  

  • 16. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome.
    Baraitser M; Winter RM
    J Med Genet; 1988 Jan; 25(1):41-3. PubMed ID: 3351890
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal recessive Robinow syndrome.
    Teebi AS
    Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Letter: Renpenning's syndrome.
    Steele MW; Chorazy AL
    Lancet; 1974 Apr; 1(7860):752-3. PubMed ID: 4132492
    [No Abstract]   [Full Text] [Related]  

  • 19. Familial occurrence of the Williams syndrome.
    White RA; Preus M; Watters GV; Fraser FC
    J Pediatr; 1977 Oct; 91(4):614-6. PubMed ID: 908984
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial achalasia, microcephaly, and mental retardation. Case report and review of literature.
    Khalifa MM
    Clin Pediatr (Phila); 1988 Oct; 27(10):509-12. PubMed ID: 3048841
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.