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Journal Abstract Search

98 related items for PubMed ID: 4126797

  • 1. X-chromosome banding in Noonan syndrome.
    Barlow MJ, Neu RL, Gardner LI.
    Am J Dis Child; 1973 Nov; 126(5):656-7. PubMed ID: 4126797
    [No Abstract] [Full Text] [Related]

  • 2. Malformative syndrome with ring chromosome 13.
    Fryns JP, Deoover J, Van den Berghe H.
    Humangenetik; 1974 Nov; 24(3):235-40. PubMed ID: 4140834
    [No Abstract] [Full Text] [Related]

  • 3. A case of a girl with a 21 ring chromosome.
    Kucerová M, Polívková Z.
    Hum Hered; 1974 Nov; 24(1):100-4. PubMed ID: 4136482
    [No Abstract] [Full Text] [Related]

  • 4. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
    Miller JQ.
    Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
    [No Abstract] [Full Text] [Related]

  • 5. A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?
    Maximilian C, Ioan DM, Fryns JP.
    Genet Couns; 1992 Nov; 3(2):115-8. PubMed ID: 1642809
    [Abstract] [Full Text] [Related]

  • 6. An 18p21q translocation in a patient with presumptive "monosomy G".
    Cohen MM, Putnam TI.
    Am J Dis Child; 1972 Dec; 124(6):908-10. PubMed ID: 4639227
    [No Abstract] [Full Text] [Related]

  • 7. [A case of Noonan's syndrome].
    Mozziconacci P, Attal C, Gorin R, Hayem F, Combourieu M, Suied B.
    Ann Pediatr (Paris); 1970 Mar 02; 17(3):220-6. PubMed ID: 5440169
    [No Abstract] [Full Text] [Related]

  • 8. [F fing chromosome (46, XY, Fr) in a boy with multiple abnormalities].
    de Grouchy J, Plachot M, Sebaoun M, Bouchard R.
    Ann Genet; 1972 Jun 02; 15(2):121-6. PubMed ID: 4537724
    [No Abstract] [Full Text] [Related]

  • 9. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE, Appadorai V, Breg WR, Howard RO.
    Birth Defects Orig Artic Ser; 1974 Jun 02; 10(8):19-25. PubMed ID: 4142400
    [No Abstract] [Full Text] [Related]

  • 10. The Noonan syndrome--a review of the clinical and genetic features of 27 cases.
    Collins E, Turner G.
    J Pediatr; 1973 Dec 02; 83(6):941-50. PubMed ID: 4148394
    [No Abstract] [Full Text] [Related]

  • 11. G-deletion syndrome II.
    Chauvel PJ, Schindeler JD, Warren RJ.
    Humangenetik; 1972 Dec 02; 14(2):164-6. PubMed ID: 5026850
    [No Abstract] [Full Text] [Related]

  • 12. Evidence for specificity of the DA/DAPI technique.
    Merkx GF, Hopman AH, Akkermans-Scholten AC, Smeets DF.
    Cytogenet Cell Genet; 1990 Dec 02; 54(1-2):62-4. PubMed ID: 1701116
    [No Abstract] [Full Text] [Related]

  • 13. Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
    Mikkelsen M, Dahl G.
    Cytogenet Cell Genet; 1973 Dec 02; 12(5):357-66. PubMed ID: 4131091
    [No Abstract] [Full Text] [Related]

  • 14. [The clinical features of the 18 q-syndrome (author's transl)].
    Feichtinger C, Glatzl J.
    Wien Klin Wochenschr; 1974 Aug 16; 86(15):441-4. PubMed ID: 4605988
    [No Abstract] [Full Text] [Related]

  • 15. Ring-G chromosome, a new G-deletion syndrome?
    Weleber RG, Hecht F, Giblett ER.
    Am J Dis Child; 1968 Apr 16; 115(4):489-93. PubMed ID: 4296014
    [No Abstract] [Full Text] [Related]

  • 16. Fluorescence study of interphase nuclei and double Y chromosomes.
    Akesson HO, Forssman H, Wahlström J.
    Hereditas; 1971 Apr 16; 69(2):213-6. PubMed ID: 4142018
    [No Abstract] [Full Text] [Related]

  • 17. The leopard (multiple lentigines) syndrome revisited.
    Gorlin RJ, Anderson RC, Moller JH.
    Laryngoscope; 1971 Oct 16; 81(10):1674-81. PubMed ID: 4398858
    [No Abstract] [Full Text] [Related]

  • 18. Chromosome banding studies in two patients with XXXXY syndrome.
    Levy CL, Sparkes RS, Carlson HE.
    J Med Genet; 1978 Aug 16; 15(4):301-5. PubMed ID: 568665
    [Abstract] [Full Text] [Related]

  • 19. A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).
    Parker CE, Donnell GN, Mavalwala J, Hurst N, Derencsenyi A.
    Clin Pediatr (Phila); 1973 Jan 16; 12(1):42-6. PubMed ID: 4345621
    [No Abstract] [Full Text] [Related]

  • 20. Ring chromosome 7 with variable phenotypic expression.
    Zackai EH, Breg WR.
    Cytogenet Cell Genet; 1973 Jan 16; 12(1):40-8. PubMed ID: 4145271
    [No Abstract] [Full Text] [Related]

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