Medicine & Life Sciences
Lamin Type A
100%
Mandibuloacral dysplasia with type A lipodystrophy
47%
Mutation
40%
Alanine
20%
Phenotype
18%
prelamin A
17%
Acro-Osteolysis
17%
Congenital Generalized Lipodystrophy
16%
Cranial Sutures
15%
Fats
15%
Lipodystrophy
13%
Skin Pigmentation
12%
Valine
12%
Menstruation
11%
Pedigree
11%
Contracture
11%
Metalloproteases
10%
Turkey
10%
Missense Mutation
10%
Zinc
9%
Haplotypes
9%
Arginine
9%
Single Nucleotide Polymorphism
8%
Complementary DNA
8%
Nucleotides
8%
Genes
8%
Neck
7%
Breast
7%
Parents
7%
Extremities
7%
Referral and Consultation
7%
Genotype
7%
Joints
7%
Health Care Outcome Assessment
6%
Chemical Compounds
Mutation
60%
Fat
23%
Alanine Residue
16%
Valine
13%
Complementary DNA
12%
Arginine
11%
Alanine
11%
Disorder
10%
Nucleotide
9%