SUMMARY A series of biochemical, staining and electron microscopy techniques were
utilized to investigate the mechanisms of C-and G-banding. These led to the following …

A cDNA coding for histatin 1 was isolated from a human submandibular-gland library and
sequenced. This cDNA was used to probe RNAs isolated from a variety of tissues to …

Standards of care are rapidly changing in clinical cytogenetics. Today's research almost
immediately becomes tomorrow's clinical test. What was once unsolvable becomes …

Here we report on three patients with dup (7p) and review the previously published 17
cases. Characteristic manifestations include severe/profound psychomotor retardation …

Multiple genetic loci have been implicated in the search for schizophrenia susceptibility
genes, none having been proven as causal. Genetic heterogeneity is probable in the …

The following is a summary of presentations given during an ancillary meeting to the 1993
American Society of Human Genetics Meeting in New Orleans, LA. This ancillary meeting …

In the Atlas of Human Chromosome Heteromorphisms, we emphasized the rapid change in
standards of care in clinical cytogenetics—“that today's research almost immediately …

Human Chromosome Variation: Heteromorphism and Polymorphism was formerly printed
under the title “Atlas of Human Chromosome Heteromorphism”. The Atlas has become a …

We report three cases of amniocentesis in which mosaicism for trisomy 12 was detected in
two or more independent cultures. The parents elected to terminate the pregnancy in all …

We describe a liveborn infant with uniparental disomy (UPD) with trisomy 15 mosaicism.
Third trimester amniocentesis yielded a 46, XX/47, XX,+ 15 karyotype. Symmetrical growth …