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 *

75 related articles for article (PubMed ID: 928031)

  • 21. Familial holoprosencephaly.
    Dallaire L; Fraser FC; Wiglesworth FW
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):136-42. PubMed ID: 5173201
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [A new autosomal-recessive hereditary syndrome. Multiple peripheral pulmonary stenosis, brachytelephalangia, inner-ear deafness, ossification or calcification of cartilages].
    Keutel J; Jörgensen G; Gabriel P
    Dtsch Med Wochenschr; 1971 Oct; 96(43):1676-81 passim. PubMed ID: 5099199
    [No Abstract]   [Full Text] [Related]  

  • 23. Japanese kindred with FG syndrome.
    Kato R; Niikawa N; Nagai T; Fukushima Y
    Am J Med Genet; 1994 Aug; 52(2):242-3. PubMed ID: 7802020
    [No Abstract]   [Full Text] [Related]  

  • 24. Noonan syndrome: a review.
    Mendez HM; Opitz JM
    Am J Med Genet; 1985 Jul; 21(3):493-506. PubMed ID: 3895929
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A new familial malformation syndrome.
    Ampola MG
    Birth Defects Orig Artic Ser; 1974; 10(7):129-35. PubMed ID: 4425370
    [No Abstract]   [Full Text] [Related]  

  • 26. Congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation: a new syndrome?
    Ramos-Arroyo MA; Clark GG; Saksena SS; Hodes ME
    Am J Med Genet; 1987 Feb; 26(2):345-54. PubMed ID: 2433942
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [The syndrome of supravalvular aortic stenosis, mental retardation and peculiar facies].
    Alsac J; Guay JM; Paquet E
    Arch Mal Coeur Vaiss; 1973 Jun; 66(6):765-73. PubMed ID: 4199790
    [No Abstract]   [Full Text] [Related]  

  • 28. [Familial pulmonary stenosis: considerations on genetic aspects].
    Manetti A; Favilli S; Mandorla S; De Simone L; Dolara A
    G Ital Cardiol; 1990 Aug; 20(8):726-8. PubMed ID: 2272419
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC; Geerdink RA; Hamel BC; Hennekam FA; Kraus P; Rammeloo JA; Tillemans AA
    Am J Med Genet; 1989 Dec; 34(4):593-600. PubMed ID: 2624276
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Seizure disorder, mental retardation, unusual facies, and abnormal hair.
    Coleman M; Randall J
    J Clin Dysmorphol; 1983; 1(3):28-9. PubMed ID: 6423779
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. Syndactyly type 1 with cataracts and mental retardation.
    Pavone L; Fiumara A; Rizzo R; Parano E; Incorpora G
    Clin Dysmorphol; 1993 Jul; 2(3):257-9. PubMed ID: 8287189
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The 18p- syndrome. Report of five cases.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Williams (Elfin Facies) syndrome: review of the literature and report of a rare case.
    Boraz RA
    ASDC J Dent Child; 1991; 58(1):57-9. PubMed ID: 2033166
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Coffin-Siris syndrome. Critical study of the literature apropos of a case].
    Foasso MF; Hermier M; Descos B; Collet JP; Perron F
    Pediatrie; 1983 Mar; 38(2):111-7. PubMed ID: 6622139
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A new syndrome of familial short stature, small hands, valvular heart disease and a characteristic facies.
    Collins FA; Partington MW; Mulcahy D; Turner G
    Clin Genet; 1990 Jan; 37(1):18-23. PubMed ID: 2302822
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Costello syndrome: the natural history of a true postnatal growth retardation syndrome.
    Umans S; Decock P; Fryns JP
    Genet Couns; 1995; 6(2):121-5. PubMed ID: 7546454
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. [The familial genesis of peripheral pulmonary stenosis (author's transl)].
    Hoshino Y; Takada K; Fujiwara T; Karino K; Nishimura S; Kamata K; Komatsu S
    Kokyu To Junkan; 1981 Jan; 29(1):101-7. PubMed ID: 7255955
    [No Abstract]   [Full Text] [Related]  

  • 40. [A new cleft lip/palate syndrome associated with mental retardation, unusual facies and skeletal anomalies (author's transl)].
    Friedman E; Kleiner A; Wolpe C; Hertz M; Goodman RM
    Schweiz Rundsch Med Prax; 1980 Nov; 69(46):1689-91. PubMed ID: 7267595
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.