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 *

145 related articles for article (PubMed ID: 5016336)

  • 21. Turner syndrome and Noonan's syndrome.
    Summitt RL
    J Pediatr; 1969 Oct; 75(4):730-1. PubMed ID: 5809851
    [No Abstract]   [Full Text] [Related]  

  • 22. Turner phenotype: mosaic 45,X-47,XY, plus 18.
    Schinzel A; Schmid W; Prader A
    J Med Genet; 1974 Mar; 11(1):101-4. PubMed ID: 4135076
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Two sisters with major gonadal dysgenesis, dwarfism, microcephaly, arachnodactyly, and normal karyotype 46, XX].
    Maximilian C; Ionescu B; Bucur A
    J Genet Hum; 1970 Dec; 18(4):365-78. PubMed ID: 5524817
    [No Abstract]   [Full Text] [Related]  

  • 24. [Cutis verticis gyrata in a newborn infant].
    Hernández Rastrollo R; Martínez Tallo E; Galan Gómez E; Cardesa García JJ
    An Esp Pediatr; 1993 Nov; 39(5):466-7. PubMed ID: 8285472
    [No Abstract]   [Full Text] [Related]  

  • 25. [The role of genetic factors in the etiology of anomalies of permanent tooth root].
    Beliakov IuA; Aubov AA; Titov VI
    Stomatologiia (Mosk); 1974; 53(6):54-7. PubMed ID: 4531753
    [No Abstract]   [Full Text] [Related]  

  • 26. Turner syndrome: the Leuven experience (1965-1989) in 478 patients. I. Patient's age at the time of diagnosis in relation to chromosomal findings.
    Kleczkowska A; Kubien E; Fryns JP; Van den Berghe H
    Genet Couns; 1990; 1(3-4):235-40. PubMed ID: 2098047
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Trisomy 4p in a family with A t(4;15).
    Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ
    Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Noonan's syndrome (cardiofacial syndrome) associated with pulmonary valve dysplasia].
    Taguchi K; Kato K; Hirao M; Mochizuki T; Nakagaki M
    Kyobu Geka; 1975 Apr; 28(4):252-8. PubMed ID: 1171315
    [No Abstract]   [Full Text] [Related]  

  • 29. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
    Hustinx TW; Haar BG; Scheres JM; Rutten FJ
    Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287
    [No Abstract]   [Full Text] [Related]  

  • 30. Ambiguous genitalia in neonates: a 4-year prospective study in a localized area.
    Al-Mulhim AN; Kamal HM
    East Mediterr Health J; 2010 Feb; 16(2):214-7. PubMed ID: 20799577
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Undiagnosed syndrome of psychomotor retardation, low birthweight dwarfism, skeletal, dental, dermal and genital anomalies.
    Elliott DE
    Birth Defects Orig Artic Ser; 1975; 11(2):364-7. PubMed ID: 1241660
    [No Abstract]   [Full Text] [Related]  

  • 32. The Aarskog syndrome in three brothers.
    Funderburk SJ; Crandall BF
    Clin Genet; 1974; 6(2):119-24. PubMed ID: 4430151
    [No Abstract]   [Full Text] [Related]  

  • 33. Eccentric ventricular hypertrophy in familial and sporadic instances of 46 XX, XY Turner phenotype.
    Ehlers KH; Engle MA; Levin AR; Deely WJ
    Circulation; 1972 Mar; 45(3):639-52. PubMed ID: 5012250
    [No Abstract]   [Full Text] [Related]  

  • 34. Increasing role of cytogenetics in pediatric practice.
    Dayakar S; Rani DS; Babu SJ; Srilatha K; Jayanthi U; Goud KI; Jain D; Raina V
    Genet Test Mol Biomarkers; 2010 Apr; 14(2):197-204. PubMed ID: 20384456
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cardiovascular malformations in Turner's and Noonan's syndrome.
    Van der Hauwaert LG; Fryns JP; Dumoulin M; Logghe N
    Br Heart J; 1978 May; 40(5):500-9. PubMed ID: 656215
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tooth crown size and morphology in Turner syndrome.
    Midtbø M; Halse A
    Acta Odontol Scand; 1994 Feb; 52(1):7-19. PubMed ID: 8184682
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Noonan's syndrome and cryptorchidism.
    Redman JF
    J Urol; 1973 May; 109(5):909-11. PubMed ID: 4144677
    [No Abstract]   [Full Text] [Related]  

  • 38. [The Shereshevskii--Turner syndrome in monozygotic twins].
    Zarubina NA; Blagoveshchenskaia TA; Glikman EV; Tsyvilskaia LA
    Probl Endokrinol (Mosk); 1975; 21(5):37-42. PubMed ID: 1241718
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Camptomelic dwarfism associated with XY-gonadal dysgenesis and chromosome anomalies.
    Hoefnagel D; Wuster-Hill DH; Dupree WB; Benirschke K; Fuld GL
    Clin Genet; 1978 Jun; 13(6):489-99. PubMed ID: 566645
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Kabuki make-up syndrome: abnormalities of the fingertips and cutaneous hyperelasticity].
    Stalder JF; David A; Amoric JC; Bureau B; Litoux P
    Ann Dermatol Venereol; 1991; 118(11):784-5. PubMed ID: 1789630
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.