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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

279 related items for PubMed ID: 4238802

  • 1. Application of dermatoglyphical studies in medical diagnosis.
    Mutalik GS, Lokhandwala VA.
    J Assoc Physicians India; 1968 Dec; 16(12):925-32. PubMed ID: 4238802
    [No Abstract] [Full Text] [Related]

  • 2. [Diseases and dermatoglyphics].
    Shiono H.
    Nihon Hoigaku Zasshi; 1970 Nov; 24(6):446-54. PubMed ID: 4252188
    [No Abstract] [Full Text] [Related]

  • 3. [Clinical chromosome studies].
    Ganner E.
    Wien Klin Wochenschr; 1968 Oct 11; 80(41):755-7 passim. PubMed ID: 4236317
    [No Abstract] [Full Text] [Related]

  • 4. [Dermatoglyphics in medical genetics].
    Saldanha PH.
    Rev Paul Med; 1968 Apr 11; 72(4):173-204. PubMed ID: 4232847
    [No Abstract] [Full Text] [Related]

  • 5. [Clinically important chromosome aberrations].
    Pelz L.
    Z Gesamte Inn Med; 1967 Mar 15; 22(6):Suppl:83-5. PubMed ID: 4232904
    [No Abstract] [Full Text] [Related]

  • 6. [Congenital anomaly and chromosome examination].
    Fujiki N, Nakajima K.
    Rinsho Byori; 1966 Nov 15; 14(11):739-45. PubMed ID: 4227278
    [No Abstract] [Full Text] [Related]

  • 7. [Significance of dermatoglyphics in clinical practice].
    Kacejová M.
    Bratisl Lek Listy; 1970 Nov 15; 53(6):710-23. PubMed ID: 4247314
    [No Abstract] [Full Text] [Related]

  • 8. [Indications for chromosome analysis from the pediatric viewpoint].
    Steinbicker V, Braun HS, Hemke G, Euchler HB.
    Kinderarztl Prax; 1973 Feb 15; 41(2):91-8. PubMed ID: 4267824
    [No Abstract] [Full Text] [Related]

  • 9. [Cytogenetics. Importance, limitations and prospects].
    Milani-Comparetti M.
    Minerva Med; 1978 Mar 17; 69(13):885-94. PubMed ID: 148012
    [No Abstract] [Full Text] [Related]

  • 10. Human chromosome analysis.
    Centerwall WR, Murdoch JL.
    Am Fam Physician; 1975 Apr 17; 11(4):76-89. PubMed ID: 123406
    [No Abstract] [Full Text] [Related]

  • 11. [The importance of configurations or papillary lines in the identification of chromosomal diseases].
    Rott HD.
    Folia Clin Int (Barc); 1969 Oct 17; 19(10):500-6. PubMed ID: 5396731
    [No Abstract] [Full Text] [Related]

  • 12. Clinical significance and genetics of epidermal ridges--a review of dermatoglyphics.
    Verbov J.
    J Invest Dermatol; 1970 Apr 17; 54(4):261-71. PubMed ID: 4245201
    [No Abstract] [Full Text] [Related]

  • 13. [Diagnosis of chromosomal diseases].
    Davidenkova EF, Ponomarenko AM, Verlinskaiia DK.
    Klin Med (Mosk); 1966 Jan 17; 44(1):11-3. PubMed ID: 4228489
    [No Abstract] [Full Text] [Related]

  • 14. [Papillary ridges and disease].
    Wendt GG, Rube M, Kindermann I.
    Dtsch Med Wochenschr; 1971 Jun 11; 96(24):1056-62. PubMed ID: 4252998
    [No Abstract] [Full Text] [Related]

  • 15. [The practicing physician facing current problems in genetics].
    Juillard E, Grosset L.
    Rev Med Suisse Romande; 1973 Sep 11; 93(9):655-68. PubMed ID: 4272167
    [No Abstract] [Full Text] [Related]

  • 16. [Indications for chromosome analysis].
    Pfeiffer RA.
    Fortschr Med; 1985 Jan 17; 103(3):33-6. PubMed ID: 3156080
    [No Abstract] [Full Text] [Related]

  • 17. [Clinical picture of human chromosome diseases and role of supernumary chromosome heterochromatin].
    Davidenkova EF, Verlinskaia DK, Tysiachniuk SF.
    Genetika; 1974 Jan 17; 10(1):152-62. PubMed ID: 4283367
    [No Abstract] [Full Text] [Related]

  • 18. Antenatal diagnosis of genetic defects.
    Goodner DM.
    J Reprod Med; 1973 Jun 17; 10(6):261-8. PubMed ID: 4268364
    [No Abstract] [Full Text] [Related]

  • 19. [Indications for chromosome analysis in childhood].
    Goetz P, Kucerová M, Macek M.
    Cesk Pediatr; 1970 Apr 17; 25(4):161-5. PubMed ID: 4245790
    [No Abstract] [Full Text] [Related]

  • 20. 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; 17(4):225-34. PubMed ID: 4281287
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.