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Search Results - Adanur Saglam, Kübra
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A new case of Turnpenny‐Fry syndrome
by
Ercoskun, Pelin
,
Yuce Kahraman, Cigdem
,
Adanur Saglam, Kübra
,
Kanjee, Momen
,
Tatar, Abdulgani
Published in
American journal of medical genetics. Part A
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An Unusual Case of Neonatal Hypotonia and Femur Fracture: Neuromuscular Variant of Glycogen Storage Disease Type IV
by
Bezirganoglu, Handan
,
Adanur Saglam, Kubra
Published in
Children (Basel)
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A Strong Candidate Gene for Nonsyndromic Intellectual Disability Phenotype: SGSM3
by
Turkyilmaz, Ayberk
,
Saglam, Kubra Adanur
,
Yilmaz, Mustafa
,
Cebi, Alper Han
Published in
Clinical genetics
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Secondary findings in genes related to cancer phenotypes in Turkish exome sequencing data from 2020 individuals
by
Demir, Oguzhan
,
Saglam, Kubra Adanur
,
Yilmaz, Mustafa
,
Apuhan, Tuna
,
Cebi, Alper Han
,
Turkyilmaz, Ayberk
Published in
American journal of medical genetics. Part A
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A new case of Turnpenny-Fry syndrome
by
Ercoskun, Pelin
,
Yuce Kahraman, Cigdem
,
Adanur Saglam, Kübra
,
Kanjee, Momen
,
Tatar, Abdulgani
Published in
American journal of medical genetics. Part A
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An Unusual Case of Neonatal Hypotonia and Femur Fracture: Neuromuscular Variant of Glycogen Storage Disease Type IV
by
Bezirganoglu, Handan
,
Adanur Saglam, Kubra
Published in
Children (Basel, Switzerland)
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