🏷️ LIMITED TIME OFFER: GET 20% OFF GRADE+ YEARLY SUBSCRIPTION β†’
Log in
Biology
2
answers
0
watching
257
views
30 Oct 2018

(5) What is the most likely pattern of inheritance in this pedigree?

A Autosomal recessive

B X-linked recessive

C Mitochondrial

D Autosomal dominant

E X-linked dominant

Watch
2
answers
0
watching
257
views

For unlimited access to Homework Help, a Homework+ subscription is required.

4 Apr 2023

Unlock all answers

Get 1 free homework help answer.
Already have an account? Log in
Share
Already have an account? Log in
Share

Related textbook solutions

Molecular Cell Biology
8 Edition,
Lodish
ISBN: 9781464183393
Biology: Science for Life with Physiology
6 Edition,
Belk
ISBN: 9780134555430
Concepts of Biology
OER Edition,
Openstax
ISBN: 9781938168116
Biology
2nd Edition, 2013
Openstax
ISBN: 9781947172517
Essentials of Biology
5 Edition,
Mader
ISBN: 9781259660269

Related questions

1) a mutation occurs in which an AAA codon, which signifieslysine, into AGA which signifies a chemically similar amino acidarginine. This is an example of a ____ mutation?

a) conservative nonsynomous b) frameshift c)nonsense d) conditional e) silent

It has to be neutral mutation, but the option for neutral is notgiven... would it be conditional?

2) Which of the following types of inheritance could account foran affected male having all affected daugters but no affectedsons?

a) autosomal recessive b) autosomaldominant c) Y-linked d) X-linkedrecessive e) X-linked dominant

it has to be dominant... so its either b or e?

3) The site where RNA polymerase binds to the DNA template iscalled the ____ sequence.

a)

enhancer
b)

promoter
c)

domain
d)

terminator
e)

reading frame

Given their modes of inheritance, and assuming Mendelian inheritance, if a heterozygote carrier for BRCA1 (autosomal dominant) and TP53 (autosomal recessive) mated with another heterozygote carrier for BRCA1 and TP53, what is the probability of them having a child that has breast cancer, but doesnҀ™t have adrenal cortical carcinoma?

Match the following genetic disorders with each definitions. Not all choices has to be used.

Unequal crossing over during meiosis causes the chromosome missing some genes

Chromosomal mutations resulting in doubling of a part of a chromosome

An inverted chromosomal segment fractured from a chromosome is inserted at the newly created sticky ends of the same chromosome.

Breaks at the extreme ends of the short arms of two nonhomologousacrocentric chromosomes, and the small fragments produced are lost but the larger ones fuse together at their centromeric regions

Turner syndrome (45X0) and Klinefeltersyndrome (XXY)
.

95% of Down syndrome cases

Angelman syndrome

3-4% of Down syndrome cases
A.

Recessive sex-linked disease
B.

Inversion
C.

Deletion
D.

Duplications
E.

Sex-chromosome aneuploidy
F.

Dominant sex-linked disease
G.

Autosomal dominant
H.

Translocation
I.

Autosomal aneuploidy
J.

Autosomal recessive

Weekly leaderboard

Home
Homework Help 3,900,000
Biology 460,000
Start filling in the gaps now
Log in