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| Developmental Delay and Rehabilitation in an Infant with Partial Trisomy 1q32.1 to 1q44: A Case Report |
| Woo Kyung Kim, Na Mi Lee, In Seok Lim, Soo Ahn Chae, Sin Weon Yun, Dae Yong Yi, Su Yeong Kim |
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Neonatal Med. 2022;29(2):91-95. Published online May 31, 2022 DOI: https://doi.org/10.5385/nm.2022.29.2.91 |
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Developmental Delay and Rehabilitation in an Infant with Partial Trisomy 1q32.1 to 1q44: A Case Report Neonatal Medicine. 2022;29(2):91-95  Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement Prenatal Diagnosis. 2002;22(11):957-961 Partial Trisomy 3p and Partial Monosomy 11q Associated with Atrial Septal Defect, Cleft Palate, and Developmental Delay: A Case Report Cytogenetic and Genome Research. 2011;134(4):319-324 Case Report: Identification of a de novo Microdeletion 1q44 in a Patient With Seizures and Developmental Delay Frontiers in Genetics. 2021;12: Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay Cytogenetic and Genome Research. 2015;145(1):14-18 Case report: Compound heterozygous mutations in AP4M1 gene identified in a Chinese infant with Infantile Spasms and Global developmental delay . 2021; Developmental delay and multiple congenital anomalies in a child with a unique combination of partial monosomy 18 and partial trisomy 16 Developmental Medicine & Child Neurology. 2007;43(2):130-132 Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder . 2020; Developmental delay and multiple congenital anomalies in a child with a unique combination of partial monosomy 18 and partial trisomy 16 Developmental Medicine and Child Neurology. 2001;43(02):130 Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder . 2020; |
