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Freire, Bruna Lucheze
7  Ergebnisse:
Personensuche X
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1

High frequency of genetic/epigenetic disorders in short sta..:

Freire, Bruna Lucheze ; Homma, Thais Kataoka ; Lerario, Antônio Marcondes...
American Journal of Medical Genetics Part A.  188 (2022)  9 - p. 2599-2604 , 2022
Link: https://doi.org/10.1002/..
 
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2

Burden of Rare Copy Number Variants in Microcephaly: A Braz..:

Tolezano, Giovanna Cantini ; Bastos, Giovanna Civitate ; da Costa, Silvia Souza...
Journal of Autism and Developmental Disorders.  54 (2022)  3 - p. 1181-1212 , 2022
Link: https://doi.org/10.1007/..
 
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3

MON-333 Cutaneous Skeletal Hypophosphatemic Syndrome (Cshs)..:

Cabral, Hially R ; Martin, Regina Matsunaga ; Jorge, Alexander Augusto de Lima...
Journal of the Endocrine Society.  4 (2020)  Supplement_1 - p. , 2020
Link: https://doi.org/10.1210/..
 
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4

Genetic Disorders in Prenatal Onset Syndromic Short Stature..:

Homma, Thais Kataoka ; Freire, Bruna Lucheze ; Honjo Kawahira, Rachel Sayuri...
The Journal of Pediatrics.  215 (2019)  - p. 192-198 , 2019
Link: https://doi.org/10.1016/..
 
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5

MON-333 Cutaneous Skeletal Hypophosphatemic Syndrome (Cshs)..:

Maia, Thamiris Freitas ; Freire, Bruna Lucheze ; Rodrigues, Andresa de Santi...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207641/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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6

Two Patients with Severe Short Stature due to a FBN1 mutati..:

de Bruin, Christiaan ; Finlayson, Courtney ; Funari, Mariana F.A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135661/.  , 2016
Link: http://www.ncbi.nlm.nih...
 
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7

SUN-246 Low Frequency of Pathogenic Allelic Variants in the..:

Braga, Barbara ; Gomes, Nathalia ; Lerario, Antonio...
Journal of the Endocrine Society.  3 (2019)  Supplement_1 - p. , 2019
Link: https://doi.org/10.1210/..
 
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