scholarly article | Q13442814 |
P2093 | author name string | B. B. MUKHERJEE | |
O. R. MILLER | |||
W. R. BREG | |||
P2860 | cites work | Chromosome preparations of leukocytes cultured from human peripheral blood | Q34249378 |
Chromosomal aberrations in human disease. A review of the status of cytogenetics in medicine | Q35310749 | ||
THE HUMAN CHROMOSOMAL SATELLITES IN NORMAL PERSONS AND IN TWO PATIENTS WITH MARFAN'S SYNDROME | Q36433290 | ||
Heterochromatin and the organization of nucleoli in plants. | Q51056647 | ||
Constrictions in normal human chromosomes | Q78814905 | ||
Observations on the satellited human chromosomes | Q78835077 | ||
Nucleolus-organisers in the causation of chromosomal anomalies in man | Q78952615 | ||
Recent developments in human cytogenetics | Q79074481 | ||
The diagnosis of chromosome abnormalities in newborn infants by the use of umbilical cord blood cultures. I. Mongolism | Q79074482 | ||
Enlarged satellites and multiple malformations in the same pedigree | Q79382402 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | ecology | Q7150 |
karyotype | Q189967 | ||
P304 | page(s) | 372-382 | |
P577 | publication date | 1962-02-01 | |
P1433 | published in | Transactions of the New York Academy of Sciences | Q15766642 |
P1476 | title | Normal variations in the human karyotype | |
P478 | volume | 24 |
Q35231238 | Atypical acrocentric chromosomes in Negro and Caucasian Mongols |
Q35202425 | Chromosome polymorphism and twin zygosity |
Q54050436 | Cytogenetic studies in the Hottentot population: Count distribution, report of a fragment, and preliminary description of morphology |
Q59090782 | Evidence for a ‘Folded-Fibre’ Organization in Human Chromosomes |
Q70081937 | Frequency of satelliting of the human chromosomes 21 and 22 and the identity of the mongol chromosome |
Q53715327 | Ribosomal DNA Connectives between Human Acrocentric Chromosomes |
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Q35231869 | Short arm enlargement in acrocentric chromosomes. |
Q83281570 | Some fundamental considerations in human population cytogenetics |
Q34634947 | The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+) |
Q44530058 | Variations in karyotypes of normal premature babies, new-born babies and infants |
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