The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations
E Therman, B Susman… - Annals of human …, 1989 - Wiley Online Library
The present study explores the origin of human Robertsonian translocations (RT) and the
causes of the nonrandom participation of the different acrocentrics in them. Satellite …
causes of the nonrandom participation of the different acrocentrics in them. Satellite …
The critical region on the human Xq
E Therman, R Laxova, B Susman - Human genetics, 1990 - Springer
Adult female carriers of balanced X; autosome translocations (118 cases) and of balanced X
inversions (31 cases) have been collected from the literature. Forty-five of the 118 …
inversions (31 cases) have been collected from the literature. Forty-five of the 118 …
[BOOK][B] Human chromosomes: structure, behavior, and effects
E Therman, M Susman - 2012 - books.google.com
This book, like the two previous editions, was written as an introduction to human
cytogenetics, but it could also be used as a text for a general cytogenetics course, since …
cytogenetics, but it could also be used as a text for a general cytogenetics course, since …
A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome
DW Smith, K Patau, E Therman, SL Inhorn - The Journal of pediatrics, 1960 - Elsevier
Two patients are described who died in early infancy. Each displayed similar complexes of
congenital anomalies of which the following ones were found in both: low-set and …
congenital anomalies of which the following ones were found in both: low-set and …
[BOOK][B] Human chromosomes
OJ Miller, E Therman - 2011 - books.google.com
The fourth edition of this well-known text provides students, researchers and technicians in
the area of medicine, genetics and cell biology with a concise, understandable introduction …
the area of medicine, genetics and cell biology with a concise, understandable introduction …
Cytogenetics of Bloom's syndrome
EM Kuhn, E Therman - Cancer genetics and cytogenetics, 1986 - Elsevier
The quantitative aspects of Bloom's syndrome cytogenetics are reviewed. The most
characteristic feature is an increased rate of homologous chromatid exchange, both sister …
characteristic feature is an increased rate of homologous chromatid exchange, both sister …
The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis
E Therman, B Susman - Human genetics, 1990 - Springer
We have collected from the literature adult nonmosaic women with the following aberrant X
chromosomes: Xp-(52), Xq-(67), idic (Xp-)(10), idic (Xq-)(9), and interstitial deletions (12) …
chromosomes: Xp-(52), Xq-(67), idic (Xp-)(10), idic (Xq-)(9), and interstitial deletions (12) …
47, XXX females, sex chromosomes, and tooth crown structure
L Alvesalo, E Tammisalo, E Therman - Human genetics, 1987 - Springer
Enamel thickness of the maxillary permanent central incisors and canines in seven Finnish
47, XXX females, their first-degree male and female relatives, and control males and …
47, XXX females, their first-degree male and female relatives, and control males and …
X inactivation in man: a woman with t (Xq--; 12q+).
GE Sarto, E Therman, K Patau - American journal of human …, 1973 - ncbi.nlm.nih.gov
The present patient (BJ041040) was found in a cytogenetic study of 50 patients ascertained
solely on the basis of primary amenorrhea [1]. The control group for the cytological …
solely on the basis of primary amenorrhea [1]. The control group for the cytological …
Dicentric chromosomes and the inactivation of the centromere
E Therman, C Trunca, EM Kuhn, GE Sarto - Human genetics, 1986 - Springer
The origin and behavior of human dicentric chromosomes are reviewed. Most dicentrics
between two non-homologous or two homologous chromosomes (isodicentrics), which are …
between two non-homologous or two homologous chromosomes (isodicentrics), which are …