tryptophan and Anhidrotic Ectodermal Dysplasia

tryptophan has been researched along with Anhidrotic Ectodermal Dysplasia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM	1
Freire-Maia, N	1

Other Studies

2 other study(ies) available for tryptophan and Anhidrotic Ectodermal Dysplasia

Article	Year
Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5 Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female; Foot Deformities, Congenital; Genotype; Hand Deformities, Congenital; Heterozygote; Humans; Melanosis; Mutation, Missense; Phenotype; Sequence Analysis, Protein; Thymine; Transcription Factors; Tryptophan; Tumor Suppressor Proteins	2010
A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities. American journal of human genetics, 1970, Volume: 22, Issue:4 Topics: Abnormalities, Multiple; Adolescent; Adult; Alopecia; Animals; Brazil; Breast; Child; Cleft Lip; Cleft Palate; Ear Deformities, Acquired; Ectodermal Dysplasia; Ectromelia; Electrocardiography; Electroencephalography; Growth Disorders; Heart Function Tests; Humans; Hypogonadism; Infant, Newborn; Intellectual Disability; Limb Deformities, Congenital; Male; Pedigree; Sibling Relations; Skin Abnormalities; Thyroid Gland; Tooth Abnormalities; Tryptophan	1970

Article

Year

Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5

Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female; Foot Deformities, Congenital; Genotype; Hand Deformities, Congenital; Heterozygote; Humans; Melanosis; Mutation, Missense; Phenotype; Sequence Analysis, Protein; Thymine; Transcription Factors; Tryptophan; Tumor Suppressor Proteins

2010

A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities.

American journal of human genetics, 1970, Volume: 22, Issue:4

Topics: Abnormalities, Multiple; Adolescent; Adult; Alopecia; Animals; Brazil; Breast; Child; Cleft Lip; Cleft Palate; Ear Deformities, Acquired; Ectodermal Dysplasia; Ectromelia; Electrocardiography; Electroencephalography; Growth Disorders; Heart Function Tests; Humans; Hypogonadism; Infant, Newborn; Intellectual Disability; Limb Deformities, Congenital; Male; Pedigree; Sibling Relations; Skin Abnormalities; Thyroid Gland; Tooth Abnormalities; Tryptophan

1970