Found: 18
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Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families.
- Published in:
- Journal of Cosmetic Dermatology, 2015, v. 14, n. 4, p. 268, doi. 10.1111/jocd.12159
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- Article
Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry-Based Study, 2001-2012.
- Published in:
- 2019
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- Publication type:
- journal article
A Novel <bold><italic>GMPPA </italic></bold>Mutation in Two Adult Sisters with Achalasia, Alacrima, Short Stature, Dysmorphism, and Intellectual Disability.
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- Molecular Syndromology, 2018, v. 9, n. 2, p. 110, doi. 10.1159/000485908
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- Article
Isolated postaxial polydactyly: Epidemiologic characteristics from a multicenter birth defects study.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1432, doi. 10.1002/ajmg.a.61193
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- Article
Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48451-3
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- Article
Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes.
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- Salud Pública de México, 2012, v. 54, n. 6, p. 579, doi. 10.1590/S0036-36342012000600006
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- Article
Moderate altitude as a risk factor for isolated congenital malformations. Results from a case–control multicenter–multiregional study.
- Published in:
- Birth Defects Research, 2024, v. 116, n. 7, p. 1, doi. 10.1002/bdr2.2335
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- Publication type:
- Article
A multi‐program analysis of cleft lip with cleft palate prevalence and mortality using data from 22 International Clearinghouse for Birth Defects Surveillance and Research programs, 1974–2014.
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- Birth Defects Research, 2023, v. 115, n. 10, p. 980, doi. 10.1002/bdr2.2176
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- Article
Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs.
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- Birth Defects Research, 2021, v. 113, n. 12, p. 945, doi. 10.1002/bdr2.1891
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- Publication type:
- Article
Myelomeningocele genotype–phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways.
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- Birth Defects Research, 2021, v. 113, n. 4, p. 371, doi. 10.1002/bdr2.1872
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- Article
OEIS complex: Prevalence, clinical, and epidemiologic findings in a multicenter Mexican birth defects surveillance program.
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- Birth Defects Research, 2019, v. 111, n. 11, p. 666, doi. 10.1002/bdr2.1512
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- Publication type:
- Article
Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population.
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- Clinical & Translational Investigation / Revista de Investigación Clínica, 2022, v. 74, n. 6, p. 328, doi. 10.24875/RIC.22000234
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- Publication type:
- Article
TELOMERES LENGTH VARIATIONS IN A RHEUMATOID ARTHRITIS PATIENTS COHORT AT EARLY DISEASE ONSET AND AFTER FOLLOW-UP.
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- Clinical & Translational Investigation / Revista de Investigación Clínica, 2022, v. 74, n. 4, p. 202, doi. 10.24875/RIC.22000048
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- Publication type:
- Article
CLINICAL AND GENETIC FINDINGS IN MEXICAN PATIENTS WITH DUANE ANOMALY AND RADIAL RAY MALFORMATIONS/OKIHIRO SYNDROME.
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- Clinical & Translational Investigation / Revista de Investigación Clínica, 2016, v. 68, n. 5, p. 269
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- Article
Diabetes, embarazo y defectos al nacimiento.
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- Clinical & Translational Investigation / Revista de Investigación Clínica, 2008, v. 60, n. 2, p. 107
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- Publication type:
- Article
Heterogenous Distribution of MTHFR Gene Variants among Mestizos and Diverse Amerindian Groups from Mexico.
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- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0163248
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- Article
Association of Vitamin D Receptor Polymorphisms with Osteoporosis in Mexican Postmenopausal Women.
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- Human Biology, 2003, v. 75, n. 3, p. 399, doi. 10.1353/hub.2003.0045
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- Article
Genetic Risk Determinants for Cigarette Smoking Dependence in Mexican Mestizo Families.
- Published in:
- 2016
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- Publication type:
- journal article