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Mutlu Albayrak, Hatice
71  results:
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1

From cataract to syndrome diagnosis: Revaluation of Warburg..:

Mutlu Albayrak, Hatice ; Elçioğlu, Nursel H. ; Yeter, Burcu.
American Journal of Medical Genetics Part A.  185 (2021)  8 - p. 2325-2334 , 2021
Link: https://doi.org/10.1002/..
 
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2

PIGA-related epileptic encephalopathy demonstrating intrafa..:

Perk Yucel, Peren ; Mutlu Albayrak, Hatice
Acta Neurologica Belgica.  120 (2020)  5 - p. 1247-1250 , 2020
Link: https://doi.org/10.1007/..
 
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3

Kosaki Overgrowth Syndrome: Report of a Family with a Novel..:

Mutlu Albayrak, Hatice ; Calder, Alistair D
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832207/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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4

From cataract to syndrome diagnosis: Revaluation of Warburg..:

Mutlu Albayrak, Hatice ; Elçioğlu, Nursel H ; Yeter, Burcu.
American Journal of Medical Genetics, Part A.  , 2021
Link: https://hdl.handle.net/1..
 
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5

Pseudodiastrophic dysplasia expands the known phenotypic sp..:

Byrne, Alicia B ; Mizumoto, Shuji ; Arts, Peer...
Journal of Medical Genetics.  57 (2020)  7 - p. 454-460 , 2020
Link: https://doi.org/10.1136/..
 
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6

Phenotypic Overlap of Roberts and Baller-Gerold Syndromes i..:

Colombo, Elisa Adele ; Mutlu-Albayrak, Hatice ; Shafeghati, Yousef...
Frontiers in Pediatrics.  7 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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7

Vocal cord immobility as a cause of aphonia in a child with..:

Mutlu-Albayrak, Hatice ; Karaer, Kadri
International Journal of Pediatric Otorhinolaryngology.  117 (2019)  - p. 179-181 , 2019
Link: https://doi.org/10.1016/..
 
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8

Childhood-onset autosomal recessive ataxias: a cross-sectio..:

Mutlu-Albayrak, Hatice ; Kırat, Emre ; Gürbüz, Gürkan
neurogenetics.  21 (2019)  1 - p. 59-66 , 2019
Link: https://doi.org/10.1007/..
 
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9

Fetal Valproate Syndrome:

Mutlu-Albayrak, Hatice ; Bulut, Cahide ; Çaksen, Hüseyin
Pediatrics & Neonatology.  58 (2017)  2 - p. 158-164 , 2017
Link: https://doi.org/10.1016/..
 
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10

Bir doğuştan kraniyal disinnervasyon bozukluğu: Moebius sen..:

Mutlu Albayrak, Hatice ; Emiroğlu, Nuriye ; Altunhan, Hüseyin..
Türk Pediatri Arşivi.  , 2017
Link: https://hdl.handle.net/2..
 
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11

Identification ofSLC22A5Gene Mutation in a Family with Carn..:

Mutlu-Albayrak, Hatice ; Bene, Judit ; Oflaz, Mehmet Burhan...
Case Reports in Genetics.  2015 (2015)  - p. 1-5 , 2015
Link: https://doi.org/10.1155/..
 
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12

Evaluation of the Neurodevelopmental Status for Urea Cycle ..:

Ayşe Ergül Bozacı ; Emine Göksoy ; Aysel Tekmenuray Ünal...
http://jpedres.org/archives/archive-detail/article-preview/evaluation-of-the-neurodevelopmental-status-for-ur/62076.  , 2023
Link: https://doi.org/10.4274/..
 
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13

SCUBE3 loss-of-function causes a recognizable recessive dev..:

Lin, Yuh-Charn ; Niceta, Marcello ; Muto, Valentina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820739/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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14

The Spectrum of NF1 Gene Variations in Southeastern Turkey:

Emre Kırat ; Hatice Mutlu Albayrak
http://jpedres.org/archives/archive-detail/article-preview/the-spectrum-of-inf1-i-gene-variations-in-southeas/48644.  , 2021
Link: https://doi.org/10.4274/..
 
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15

The Genomics of Arthrogryposis, a Complex Trait: Candidate ..:

Pehlivan, Davut ; Bayram, Yavuz ; Gunes, Nilay...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612529/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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