Issue Information

Assisted reproduction and congenital malformations: A systematic review and meta‐analysis
di: Meenakshi Veeramani, et al.
Pubblicazione: (2024)

A case series study on the safety of cefditoren pivoxil use during the first trimester of pregnancy in Japan
di: Mariko Honma, et al.
Pubblicazione: (2024)

Acoustic evaluation of voice signal distortion by videoconferencing platforms and devices used in telepractice for cleft palate
di: Shiho Tajiri, et al.
Pubblicazione: (2024)

Questionnaire survey on public awareness of cleft lip with/without palate in Mongolia
di: Anar‐Erdene Gantugs, et al.
Pubblicazione: (2024)

Risk of major birth defects after first‐trimester exposure to carbocisteine and ambroxol: A multicenter prospective cohort study using counseling data for drug safety during pregnancy
di: Mariko Usuda, et al.
Pubblicazione: (2024)

Risk factors for isolated congenital heart defects in infants from Western Mexico
di: Jessica Paola Cruz‐Cruz, et al.
Pubblicazione: (2024)

Pyramidalis muscle formation during human embryonic and early fetal periods
di: Yui Iwasa, et al.
Pubblicazione: (2024)

Congenital cardiac anomalies in non‐syndromic cleft lip and cleft palate patients: A systematic review and meta‐analysis
di: Bindey Kumar, et al.
Pubblicazione: (2024)

Upper airway obstruction due to congenital epiglottic cyst: Report of two cases
di: Kensuke Uraguchi, et al.
Pubblicazione: (2024)

The role of sonic hedgehog signaling in the oropharyngeal epithelium during jaw development
di: Rika Takeuchi, et al.
Pubblicazione: (2024)

Accumulation of ether phospholipids in induced pluripotent stem cells and oligodendrocyte‐lineage cells established from patients with Sjögren‐Larsson syndrome
di: Yu Yamaguchi, et al.
Pubblicazione: (2024)

Ultrasound and magnetic resonance imaging features of fetal urogenital anomalies: A pictorial essay
di: Behnaz Moradi, et al.
Pubblicazione: (2024)

Long‐term follow‐up for the atypical radial longitudinal deficiency: A case report
di: Hiroshi Satake, et al.
Pubblicazione: (2024)

Feelings and thoughts about life selection in pregnant women undergoing non‐invasive prenatal testing in Japan
di: Eri Takeda, et al.
Pubblicazione: (2024)

Non‐progressive hepatic tumor with high levels of serum alpha‐fetoprotein in two infants with trisomy 18
di: Toshio Okamoto, et al.
Pubblicazione: (2024)

Difficulties in disclosing secondary findings by facilities performing comprehensive germline genetic testing for rare diseases in Japan
di: Kana Hiromoto, et al.
Pubblicazione: (2024)

Genitourinary and craniofacial/cervicothoracic anomalies in a neonate with in‐utero mycophenolate mofetil exposure
di: Sayu Omori‐Shimano, et al.
Pubblicazione: (2024)

Height difference between the right and left metanephroi during early human fetal development
di: Hana Ishiyama‐Takara, et al.
Pubblicazione: (2024)

Acknowledgement
Pubblicazione: (2024)

A safety signal for congenital strabismus associated with valproic acid: A pharmacovigilance analysis utilizing the FDA Adverse Event Reporting System database
di: Yuichi Uwai, et al.
Pubblicazione: (2024)

Early prenatal diagnosis of spondylocostal dysostosis caused by a novel variant in MESP2
di: Yanhong Zhou, et al.
Pubblicazione: (2024)

A novel 2.4‐kb PHKA2 deletion in a boy with glycogen storage disease type IXa
di: Takeshi Sato, et al.
Pubblicazione: (2024)

A novel variant in IFT122 associated with a severe phenotype of cranioectodermal dysplasia
di: Shiho Nagayama, et al.
Pubblicazione: (2024)

A Case of HNRNPU ‐Related Neurodevelopmental Disorder Presenting With Acute Encephalopathy and Basal Ganglia Lesions
di: Syunsuke Nagara, et al.
Pubblicazione: (2026)

Severe pharyngeal stenosis and laryngomalacia in an individual of HNRNPU ‐related neurodevelopmental disorder associated with a novel nonsense variant
di: Yusuke Sasaki, et al.
Pubblicazione: (2025)

Non‐Immune Hydrops Fetalis, Multifocal Chorangiomatosis, and Noonan Syndrome 8
di: Eugen‐Matthias Strehle, et al.
Pubblicazione: (2025)

Morphogenesis of the Extraocular Muscles During the Human Embryonic and Early Fetal Periods
di: Miho Osaka, et al.
Pubblicazione: (2026)

Postnatal Bimodal Dynamics and Androgen‐Induced Masculinization of the External Genitalia in Mice
di: Junki Aikawa, et al.
Pubblicazione: (2026)

Urinary Metabolic Screening Misled the Molecular Diagnosis of Xia–Gibbs Syndrome
di: Sayaka Enomoto, et al.
Pubblicazione: (2026)

Morphological relationship between the cranial base and facial anomalies in humans: Challenges and future perspectives
di: Natsuko Utsunomiya, et al.
Pubblicazione: (2025)

Predictability of fetal pulmonary artery Doppler on neonatal outcomes in pregnant women with gestational diabetes mellitus
di: Huriye Ezveci, et al.
Pubblicazione: (2025)

Compound heterozygous ZNF335 variants in a patient with microcephaly, refractory epilepsy, and severe developmental delay: A case report and literature review
di: Kaori Yamoto, et al.
Pubblicazione: (2025)

Co‐Occurrence of Urogenital Anomalies and Congenital Heart Disease in a Child With Alpha‐Thalassemia Mental Retardation Syndrome Associated With Chromosome 16 Abnormalities due to Partial Monosomy 16p13.3 and Partial Trisomy 16q22.1–q24.3
di: Hideki Tamaru, et al.
Pubblicazione: (2025)

Focused Clinical Observation of Functional Outcomes in Children With OEIS Complex
di: Osamu Yazawa, et al.
Pubblicazione: (2026)

A cohort study on structural analysis of congenital anomalies in an intensive care unit in Azerbaijan
di: Narmin Akif Azizova, et al.
Pubblicazione: (2025)

Patients With Hereditary Hemorrhagic Telangiectasia Diagnosed by Nanopore Long Read Sequencer
di: Mamiko Yamada, et al.
Pubblicazione: (2025)