Catalogue of Unbalanced Chromosome Aberrations in Man
eBook - PDF

Catalogue of Unbalanced Chromosome Aberrations in Man

Albert Schinzel

Share book
  1. 933 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Catalogue of Unbalanced Chromosome Aberrations in Man

Albert Schinzel

Book details
Book preview
Table of contents
Citations

Frequently asked questions

How do I cancel my subscription?
Simply head over to the account section in settings and click on “Cancel Subscription” - it’s as simple as that. After you cancel, your membership will stay active for the remainder of the time you’ve paid for. Learn more here.
Can/how do I download books?
At the moment all of our mobile-responsive ePub books are available to download via the app. Most of our PDFs are also available to download and we're working on making the final remaining ones downloadable now. Learn more here.
What is the difference between the pricing plans?
Both plans give you full access to the library and all of Perlego’s features. The only differences are the price and subscription period: With the annual plan you’ll save around 30% compared to 12 months on the monthly plan.
What is Perlego?
We are an online textbook subscription service, where you can get access to an entire online library for less than the price of a single book per month. With over 1 million books across 1000+ topics, we’ve got you covered! Learn more here.
Do you support text-to-speech?
Look out for the read-aloud symbol on your next book to see if you can listen to it. The read-aloud tool reads text aloud for you, highlighting the text as it is being read. You can pause it, speed it up and slow it down. Learn more here.
Is Catalogue of Unbalanced Chromosome Aberrations in Man an online PDF/ePUB?
Yes, you can access Catalogue of Unbalanced Chromosome Aberrations in Man by Albert Schinzel in PDF and/or ePUB format, as well as other popular books in Medicina & Genética en medicina. We have over one million books available in our catalogue for you to explore.

Information

Publisher
De Gruyter
Year
2020
ISBN
9783112329047
Edition
1
83 
9
years 
old. 
Many 
of 
the 
features 
mentioned 
above 
are 
also 
consistently 
found 
in 
the 
"18p— 
syndrome", 
compli-
cating 
the 
correlation 
of 
the 
phenotype 
of 
partial 
dup-
lication 
of 
lq 
and 
deletion 
of 
the 
other 
chromosome. 
Another 
family 
member 
with 
cebocephaly 
died 
early. 
Var-
ying 
degrees 
of 
arrhinencephaly 
are 
common 
in 
del(18p); 
however, 
cyclopia 
and 
cebocephaly 
have 
also 
been 
obser-
ved 
in 
patients 
with 
the 
dup(l) 
(q32-*qter) 
*Liberfarb 
R.M., 
Breg 
W.R., 
Atkins 
L., 
et 
al.: 
Multiple 
congenital 
anomalies/mental 
retardation(MCA/MR) 
syndrome 
due 
to 
partial 
lq 
duplication 
and 
possible 
18p 
deletion: 
study 
of 
four 
individuals 
in 
two 
families. 
Am.J.Med.Genet. 
4,27-37(1979). 
dup(l)(q44+qter) 
Kessel 
E., 
Pfeiffer 
R.A., 
Welling 
P.: 
Translocation 
22/Y 
familiale 
et 
trisomie 
partielle 
autosomique 
chez 
une 
jeune 
fille. 
J.Genet. 
Hum. 
27,45-51(1979). 

Table of contents