Cornelia De Lange Syndrome Karyotype Collection Mode [2022] Cornelia De Lange Syndrome Karyotype Collection Mode [2022]

Cornelia De Lange Syndrome Karyotype

July 13, 2024

A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death | Journal of Clinical Pathology Frontiers | Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese Patients Cornelia de Lange syndrome: MedlinePlus Genetics Cornelia De Lange Syndrome Karyotype

The karyotype of 46,XX,del(9) (q31.1q32). The arrow at chromosome 9... | Download S…
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A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with g…
Frontiers | Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in C…
Cornelia de Lange syndrome: MedlinePlus Genetics
A 16-Day-Old Infant with a Clinical Diagnosis of Classical Cornelia de Lange Syndro…
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Prenatal diagnosis and array comparative genomic hybridization characterization of …
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NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins an…
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Classic Cornelia de Lange syndrome with variant of unknown significance detected in…
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Prenatal/neonatal pathology in two cases of Cornelia de Lange syndrome harboring no…
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Frontiers | Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in C…
A 16-Day-Old Infant with a Clinical Diagnosis of Classical Cornelia de Lange Syndro…
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Auckland boy with rare syndrome learns to walk in time for Christmas | Stuff.co.nz
Cornelia De-Lange Syndrome – New Indian Journal of Pediatrics
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Case Report: Atypical Cornelia de Lange Syndrome | F1000Research
A newborn with Cornelia de Lange syndrome: a case report | Cases Journal | Full Text
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PDF] Cornelia de Lange Syndrome: A Newborn with Imperforate Anus and a NIPBL Mutati…
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