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Petrin, Aline Lourenço
16  Ergebnisse:
Personensuche X
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1

Analysis of MLL2 gene in the first Brazilian family with Ka..:

Kokitsu‐Nakata, Nancy Mizue ; Petrin, Aline Lourenço ; Heard, Jason Paul...
American Journal of Medical Genetics Part A.  158A (2012)  8 - p. 2003-2008 , 2012
Link: https://doi.org/10.1002/..
 
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2

Monozygotic twins with variable expression of Van der Woude..:

Jobling, Rebekah ; Ferrier, Raechel A. ; McLeod, Ross...
American Journal of Medical Genetics Part A.  155 (2011)  8 - p. 2008-2010 , 2011
Link: https://doi.org/10.1002/..
 
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3

Further characterization of microdeletion syndrome involvin..:

Félix, Têmis Maria ; Petrin, Aline Lourenço ; Sanseverino, Maria Teresa Vieira.
American Journal of Medical Genetics Part A.  152A (2010)  10 - p. 2604-2608 , 2010
Link: https://doi.org/10.1002/..
 
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4

Analysis of MLL2 genein the first Brazilian family with Kab..:

Kokitsu-Nakata, Nancy Mizue ; Petrin, Aline Lourenço ; Heard, Jason Paul...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724514.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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5

Monozygotic Twins with Variable Expression of Van der Woude..:

Jobling, Rebekah ; Ferrier, Raechel A ; McLeod, Ross...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140610.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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6

Further Characterization of Microdeletion Syndrome Involvin..:

Félix, Têmis Maria ; Petrin, Aline Lourenço ; Sanseverino, Maria Teresa Vieira.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946431.  , 2010
Link: http://www.ncbi.nlm.nih...
 
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7

Damaging Mutations in AFDN Contribute to Risk of Nonsyndrom..:

Awotoye, Waheed ; Mossey, Peter A ; Hetmanski, Jacqueline B...
The Cleft Palate Craniofacial Journal.  61 (2022)  4 - p. 697-705 , 2022
Link: https://doi.org/10.1177/..
 
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8

Whole-genome sequencing reveals de-novo mutations associate..:

Awotoye, Waheed ; Mossey, Peter A. ; Hetmanski, Jacqueline B....
Scientific Reports.  12 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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9

Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saha..:

Gowans, Lord J. J. ; Comnick, Carissa L. ; Mossey, Peter A....
The Cleft Palate-Craniofacial Journal.  59 (2021)  7 - p. 841-851 , 2021
Link: https://doi.org/10.1177/..
 
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10

Variant analyses of candidate genes in orofacial clefts in ..:

Li, Mary ; Olotu, Joy ; Buxo‐Martinez, Carmen J....
Oral Diseases.  28 (2021)  7 - p. 1921-1935 , 2021
Link: https://doi.org/10.1111/..
 
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11

Variant Analyses of Candidate Genes in Orofacial Clefts in ..:

Awotoye, Waheed ; Li, Mary ; Olotu, Joy...
The FASEB Journal.  35 (2021)  S1 - p. , 2021
Link: https://doi.org/10.1096/..
 
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12

Non‐random distribution of deleterious mutations in the DNA..:

Alade, Azeez A. ; Buxo‐Martinez, Carmen J. ; Mossey, Peter A....
Molecular Genetics & Genomic Medicine.  8 (2020)  8 - p. , 2020
Link: https://doi.org/10.1002/..
 
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13

Identification of Isthmin 1 as a Novel Clefting and Craniof..:

Lansdon, Lisa A ; Darbro, Benjamin W ; Petrin, Aline L...
Genetics.  208 (2018)  1 - p. 283-296 , 2018
Link: https://doi.org/10.1534/..
 
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14

Identification of 16q21 as a modifier of nonsyndromic orofa..:

Carlson, Jenna C. ; Standley, Jennifer ; Petrin, Aline...
Genetic Epidemiology.  41 (2017)  8 - p. 887-897 , 2017
Link: https://doi.org/10.1002/..
 
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15

Replication of Genome Wide Association Identified Candidate..:

Butali, Azeez ; Suzuki, Satoshi ; Cooper, Margaret E....
American Journal of Medical Genetics Part A.  161 (2013)  5 - p. 965-972 , 2013
Link: https://doi.org/10.1002/..
 
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