A survey of a familial transmission of an anomalous autosome in group 13–15

[1]  P. Jacobs,et al.  Chromosome studies on randomly chosen men and women. , 1965, Lancet.

[2]  D. Carr,et al.  MONGOLISM (DOWN'S SYNDROME) WITH ATYPICAL CLINICAL AND CYTOGENETIC FEATURES. , 1964, The Journal of pediatrics.

[3]  S. Makino.  Chromosomal studies in normal human subjects and in 300 cases of congenital disorders. , 1964, Cytologia.

[4]  Morio Sasaki.  Semigroups whose arbitrary subsets containing a definite element are subsemigroups , 1963 .

[5]  M. Sasaki,et al.  Chromosomal aberrations in congenital cardiovascular disorders of man. , 1963 .

[6]  P. Jacobs,et al.  Cytogenetic studies in leucocytes on the general population: subjects of ages 65 years and more , 1963, Annals of human genetics.

[7]  S. Walker,et al.  Familial transmission of a translocation between two chromosomes of the 13–15 group (Denver classification) , 1962 .

[8]  H. Cooper.  The use of human chromosome markers in linkage studies. , 1962, Transactions of the New York Academy of Sciences.

[9]  P. Moorhead,et al.  A familial chromosome translocation associated with speech and mental retardation. , 1961, American journal of human genetics.

[10]  P. Nowell,et al.  Chromosome preparations of leukocytes cultured from human peripheral blood. , 1960, Experimental cell research.

[11]  Tosio Kato.  Some mapping theorems for the numerical range , 1965 .

[12]  T. Omura,et al.  A Preliminary Note on an Aberrant Autosome (Group 13.15) in a Male Child and in his Father , 1965 .

[13]  M. Sasaki,et al.  A Preliminary Note on a Familial B/C Chromosome Translocation with regard to the Spontaneous Abortion , 1965 .

[14]  M. Lamy,et al.  [FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION]. , 1964, Annales de genetique.

[15]  D. Hungerford,et al.  AN ABERRANT AUTOSOME (13-15) IN A HUMAN FEMALE AND HER FATHER, BOTH APPARENTLY NORMAL. , 1963, Cytogenetics.

[16]  B. Kallen,et al.  Abnormal length of chromosomes 21 and 22 in four patients with Marfan's syndrome. , 1962, Cytogenetics.

[17]  W. Schmid.  A familial chromosome abnormality associated with repeated abortions. , 1962, Cytogenetics.