Journal Report

CLINICAL DYSMORPHOLOGY

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Journal Information
Journal Title
CLINICAL DYSMORPHOLOGY
Publisher
LIPPINCOTT WILLIAMS & WILKINS
ISSN
0962-8827
E-ISSN
1473-5717
Database
Clarivate
Domain
Health Sciences, Life Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Mucopolysaccharidoses in Morocco: a 19-year retrospective study reveals a founder mutation in mucopolysaccharidosis type I and delineates the clinical spectrum
Azzeddine Laaraje, Abdelilah Radi, Abdelhakim Ourrai et al.
2026-10-27
DOI: 10.1097/mcd.0000000000000584
Application of deep learning and explainable AI-supported medical decision-making for facial phenotyping in genetic syndromes
Ömer Sümer, Tobias Huber, Jiayi Cheng et al.
2026-10-8
DOI: 10.1097/mcd.0000000000000581
A prenatal-onset severe phenotype of SLC35A2-related congenital disorder of glycosylation associated with a mosaic hemizygous intronic variant
Yukiko Kuroda, Tomoko Saito, Yasuhiro Kawai et al.
2026-10-6
DOI: 10.1097/mcd.0000000000000583
Expanding the phenotype of GDI1-related neurodevelopmental disorder: report of the fifth family
Bryson M. Lewis, Shruti Sinha, Lois J. Starr
2026-9-29
DOI: 10.1097/mcd.0000000000000582
Second-trimester prenatal phenotype of complete trisomy 10 with combined encephalocele and myelomeningocele
Cem Terece, Osman Aydin, Şans Odabasi Aydin et al.
2026-9-29
DOI: 10.1097/mcd.0000000000000578
Marbach–Rustad progeroid syndrome caused by a hotspot LEMD2 variant: expanding the phenotypic spectrum with skeletal, cutaneous, and renal findings
Hayriye Nermin Keçeci, Ayça Burcu Kahraman, Nurdan Çiftçi et al.
2026-9-23
DOI: 10.1097/mcd.0000000000000580
Nonimmune hydrops fetalis with skeletal dysplasia due to a novel homozygous recessive TAPT1 splice-donor variant
Naren Satya Srinivas M., Shivani Mishra, Himani Pandey et al.
2026-9-14
DOI: 10.1097/mcd.0000000000000577
Developmental delay, white matter changes, and multiple endocrine hormone deficiencies in MADD-related disorders: a new case and phenotypic expansion
Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, Archana Varghese et al.
2026-9-2 Vol. 35 Issue 4 Pages 170-176
DOI: 10.1097/mcd.0000000000000574
Primrose syndrome with a novel ZBTB20 variant with congenital glaucoma and hydrocephalus
Abhinav Thakral, Robert Wallerstein
2026-9-2 Vol. 35 Issue 4 Pages 183-184
DOI: 10.1097/mcd.0000000000000566
A case of serpentine fibula-polycystic kidney syndrome presenting with foetal limb shortening: a disorder of foetal osteogenesis and part of the phenotypic spectrum of Hajdu–Cheney syndrome
Yumi Ito, Naoki Ito, Yukiko Kuroda et al.
2026-9-2 Vol. 35 Issue 4 Pages 180-182
DOI: 10.1097/mcd.0000000000000568
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Printed: November 3, 2026 02:09