287 related articles for article (PubMed ID: 5990143)
41. Symposium on intrauterine diagnosis; held at Indianapolis, Indiana, October 13 and 14, 1970. Introductory remarks.
Neel JV
Birth Defects Orig Artic Ser; 1971 Apr; 7(5):4. PubMed ID: 5120225
[No Abstract] [Full Text] [Related]
42. Genetics of childhood disorders: IX. Triplet repeat disorders.
Margolis RL; Ross CA
J Am Acad Child Adolesc Psychiatry; 1999 Dec; 38(12):1598-600. PubMed ID: 10596262
[No Abstract] [Full Text] [Related]
43. When is familial genetic?
Carter CO
Clin Gastroenterol; 1982 Jan; 11(1):3-15. PubMed ID: 7060287
[No Abstract] [Full Text] [Related]
44. Preconception and genetic counselling.
Wong HB
J Singapore Paediatr Soc; 1987; 29(3-4):75-83. PubMed ID: 3450974
[No Abstract] [Full Text] [Related]
45. [Trends in clinical genetics].
Yanase T
Nihon Rinsho; 1984 Mar; 42(3):754-66. PubMed ID: 6381805
[No Abstract] [Full Text] [Related]
46. Behavior genetics. Introduction to genetics.
Asimov I
Semin Psychiatry; 1970 Feb; 2(1):3-10. PubMed ID: 5317355
[No Abstract] [Full Text] [Related]
47. Genetic diseases.
Kirkman HN
N C Med J; 1984 Jul; 45(7):449-54. PubMed ID: 6589493
[No Abstract] [Full Text] [Related]
48. One role for genetics in ophthalmology.
Renwick JH
Trans Ophthalmol Soc U K (1962); 1970; 90():111-5. PubMed ID: 5283397
[No Abstract] [Full Text] [Related]
49. [Genetic participation in deaf-mutism].
Bartual R
Acta Otorinolaryngol Iber Am; 1969; 20(3):278-306. PubMed ID: 5816444
[No Abstract] [Full Text] [Related]
50. The impact of single gene and chromosomal disorders on hospital admissions of children and adolescents: a population-based study.
Dye DE; Brameld KJ; Maxwell S; Goldblatt J; Bower C; Leonard H; Bourke J; Glasson EJ; O'Leary P
Public Health Genomics; 2011; 14(3):153-61. PubMed ID: 21124008
[TBL] [Abstract][Full Text] [Related]
51. [Medical genetic importance of studies of human embryonic organs].
Brusilovskiĭ AI; Krivosheina GN
Tsitol Genet; 1981; 15(3):83-8. PubMed ID: 7020187
[No Abstract] [Full Text] [Related]
52. [Medical and genetic counseling for families with hereditary diseases].
Guzeev GG
Feldsher Akush; 1980; 45(7):21-7. PubMed ID: 6903498
[No Abstract] [Full Text] [Related]
53. [Hereditary factor V deficiency (parahemophilia) in a Swiss family].
López V; Pflugshaupt R; Wirthner H; Bütler R
Schweiz Med Wochenschr; 1969 Sep; 99(38):1354-6. PubMed ID: 5349532
[No Abstract] [Full Text] [Related]
54. Small accessory chromosomes (SAC) and their genotype--phenotype correlation.
Fryns JP; Kleczkowska A; Van den Berghe H
J Genet Hum; 1982 Oct; 30(3):215-32. PubMed ID: 7153768
[TBL] [Abstract][Full Text] [Related]
55. APPROACHES AND METHODS IN HUMAN GENETICS.
MCKUSICK VA
Am J Obstet Gynecol; 1964 Dec; 90():SUPPL:1014-23. PubMed ID: 14229510
[No Abstract] [Full Text] [Related]
56. [Problems of reproduction from the viewpoint of human genetics].
Lenz W
Hippokrates; 1968 Sep; 39(17):641-4. PubMed ID: 5757771
[No Abstract] [Full Text] [Related]
57. Genetics: your fate in your genes.
Matthews DR
Nurs Mirror; 1978 Oct; 147(15):30-4. PubMed ID: 250094
[No Abstract] [Full Text] [Related]
58. [Possible goals for research on congenital diseases].
Mohr J; Plum P
Ugeskr Laeger; 1968 Jun; 130(25):1045-7. PubMed ID: 5704252
[No Abstract] [Full Text] [Related]
59. Mosaicism in genetic skin disorders.
Siegel DH; Sybert VP
Pediatr Dermatol; 2006; 23(1):87-92. PubMed ID: 16445423
[No Abstract] [Full Text] [Related]
60. [Several of the principal genetics problems in pediatrics today].
Vel'tishchev IuE
Vopr Okhr Materin Det; 1972 Jun; 17(6):3-7. PubMed ID: 5069520
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
