Examples of 'is an autosomal dominant' in a sentence
Meaning of "is an autosomal dominant"
is an autosomal dominant: This phrase is commonly used in genetics to describe a trait or condition that is inherited on one of the non-sex chromosomes and will be expressed if present in the genotype
How to use "is an autosomal dominant" in a sentence
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is an autosomal dominant
The munchkin gene is an autosomal dominant one.
It is an autosomal dominant inheritance and is variable in its expressivity.
This trait occurs in humans and is an autosomal dominant trait with incomplete penetrance.
Fap is an autosomal dominant disorder caused by germline mutation in apc.
Recent research has indicated that multiple osteochondromas is an autosomal dominant inherited disease.
Marfan is an autosomal dominant disorder.
Life expectancy is not affected in HbM, which is an autosomal dominant disorder.
It is an autosomal dominant disease.
So far, what we know is that is an autosomal dominant disease.
It is an autosomal dominant inherited disease that affects both male and female.
Most family studies suggest that TS is an autosomal dominant disorder with incomplete penetrance.
HCM is an autosomal dominant disease and conventional treatments are ineffective.
Tourette 's disorder is an autosomal dominant disorder.
BS is an autosomal dominant disorder in the familial form and genetic counseling is advised.
In some embodiments, the mutation in the endogenous rhodopsin gene is an autosomal dominant mutation.
See also
Nemaline myopathy is an autosomal dominant and sometimes an autosomal recessive genetic disorder.
Progeria or Huntchinson-Gilford Syndrome is an autosomal dominant disease.
Clinodactyly is an autosomal dominant trait that has variable expressiveness and incomplete penetrance.
As stated above, EEC syndrome is an autosomal dominant disorder.
SADDAN is an autosomal dominant genetic disorder.
DETAILED DESCRIPTION Fibrodysplasia ossificans progressiva ( FOP ) is an autosomal dominant disorder of ectopic bone formation.
ARVD is an autosomal dominant trait with reduced penetrance.
The use according to claim 1, 2 or 3, wherein spinocerebellar degeneration is an autosomal dominant spinocerebellar degeneration.
The HCM is an autosomal dominant genetic disease.
Hereditary angioedema ( HAE ) types I and II is an autosomal dominant disease.
VUR is an autosomal dominant disorder.
SLC6A1 epileptic encephalopathy is an autosomal dominant genetic condition.
FOP is an autosomal dominant disorder.
Huntington 's disease abbreviated-HD, or Juvenile Huntington 's disease - JHD is an autosomal dominant disease.
HCM is an autosomal dominant condition.
Abstract, Myotonic Dystrophy of Type 1 ( DM1 ) is an autosomal dominant genetic disease.
HME is an autosomal dominant condition.
Huntington 's disease ( hd ) is an autosomal dominant neurodegenerative disease.
HD is an autosomal dominant condition.
An additional form of colon cancer is an autosomal dominant gene, hMSH2, that comprises a lesion.
This is an autosomal dominant condition resulting from a single mutation on chromosome number 7.
Abstract, Huntington 's disease ( HD ) is an autosomal dominant genetic neurodegenerative disease.
DOA is an autosomal dominant disease caused by a defect in the nuclear gene OPA1.
Familial hypertriglyceridemia is an autosomal dominant condition occurring in approximately 1 % of the population.
MH is an autosomal dominant trait that causes a severe, uncontrollable fever when anesthesia is administered.
Polycystic kidney disease (PKD3) is an autosomal dominant inheritance that leads to renal cysts.
It is an autosomal dominant disorder passing to nearly 50 % of the offspring.
Neurofibromatosis type 1 (NF1) is an autosomal dominant syndrome predisposing to malignancies.
DM1 is an autosomal dominant disorder caused by expansion of a non-coding CTG repeat in DMPK1.
Loeys - Dietz syndrome ( LDS ) is an autosomal dominant genetic connective tissue disorder.
Achondroplasia is an autosomal dominant genetic disorder with 80 % of cases identified as a sporadic mutation.
Hypertrophic cardiomyopathy HCM is an autosomal dominant disorder that affects 1 in every 500 people.
Achondroplasia is an autosomal dominant disorder, but approximately 75 % of cases represent new dominant mutations.
The Akita spontaneous mutation is an autosomal dominant mutation in the insulin II gene ( Ins2 ).
Marfan syndrome ( mfs ) is an autosomal dominant disease that affects the connective tissue.
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Women as presidents were dominant in the cantonal courts
The dominant component of those operations is mining
Examples of using Autosomal
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This is an autosomal recessive inborn error of metabolism
The condition is inherited in an autosomal recessive pattern
Autosomal dominant nocturnal frontal lobe epilepsy
