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Search Results - Berrodin, Donna
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Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment
by
Francey, Lauren J.
,
Conlin, Laura K.
,
Kadesch, Hanna E.
,
Clark, Dinah
,
Berrodin, Donna
,
Sun, Yi
,
Glessner, Joe
,
Hakonarson, Hakon
,
Jalas, Chaim
,
Landau, Chaim
,
Spinner, Nancy B.
,
Kenna, Margaret
,
Sagi, Michal
,
Rehm, Heidi L.
,
Krantz, Ian D.
Published in
American journal of medical genetics. Part A
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Duplication 12p and Pallister-Killian syndrome: A case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region
by
Izumi, Kosuke
,
Conlin, Laura K.
,
Berrodin, Donna
,
Fincher, Christopher
,
Wilkens, Alisha
,
Haldeman-Englert, Chad
,
Saitta, Sulagna C.
,
Zackai, Elaine H.
,
Spinner, Nancy B.
,
Krantz, Ian D.
Published in
American journal of medical genetics. Part A
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A Centralized Approach for Practicing Genomic Medicine
by
Biswas, Sawona
,
Medne, Livija
,
Devkota, Batsal
,
Bedoukian, Emma
,
Berrodin, Donna
,
Izumi, Kosuke
,
Deardorff, Matthew A
,
Tarpinian, Jennifer
,
Leonard, Jacqueline
,
Pyle, Loiusa
,
Gray, Christopher
,
Montgomery, Jasmine
,
Williams, Tyrah
,
Fortunato, Sierra
,
Weatherly, Jamila
,
McEldrew, Deborah
,
Kaur, Manindar
,
Raible, Sarah E
,
Wilkens, Alisha
,
Spinner, Nancy B
,
Skraban, Cara
,
Krantz, Ian D
Published in
Pediatrics (Evanston)
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American Journal Of Medical Genetics Part A
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American Journal Of Medical Genetics. Part A
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Life Sciences & Biomedicine
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Biological And Medical Sciences
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Genetics & Heredity
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Medical Genetics
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12P Duplication
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Alopecia
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Bilateral Sensorineural Hearing Loss
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Child
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Chr15Q15.3
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Chromosome Disorders - Diagnosis
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Chromosome Disorders - Genetics
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Chromosomes, Human, Pair 12 - Genetics
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Cnv
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Connexin 26
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Connexins - Genetics
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Copy Number Variation
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Delivery Of Health Care - Organization & Administration
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