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Topic Article Package: ADC (Antibody-Drug Conjugates)
An extensive collection of journal articles on antibody-drug conjugates most relevant for your research. Covering a wide range of subject areas and different cancer typologies, it supports you in accessing suited and significant journal articles appeared in renowned international top journals published by Karger.
Editorial - Late Breaking Chromosomes
Martin Poot
Original Article
Lisca Florence Wurfbain; Inge Lucia Cox; Maria Francisca van Dooren; Augusta Maria Antonia Lachmeijer; Virginie Johanna Maria Verhoeven; Johanna Maria van Hagen; Malou Heijligers; Jolien Sietske Klein Wassink - Ruiter; Saskia Koene; Saskia Mariska Maas; Hermine Elisabeth Veenstra - Knol; Johannes Kristian Ploos van Amstel; Maarten Pieter Gerrit Massink; Aebele Barber Mink van der Molen; Marie-José Henriette van den Boogaard
Triosephosphate Isomerase Deficiency: E105D Mutation in Unrelated Patients and Review of the Literature
Open Access
Arzu Selamioğlu; Meryem Karaca; Mehmet Cihan Balcı; Hüseyin Kutay Körbeyli; Aslı Durmuş; Edibe Pembegül Yıldız; Serap Karaman; Gülden Fatma Gökçay
Jong Eun Park; Sung-A Chang; Shin Yi Jang; Kyung Soo Lee; Duk-Kyung Kim; Chang-Seok Ki
A Genetics Study in the Foreskin of Boys with Hypospadias
Available to Purchase
Irem Inanc; Dincer Avlan; Damla Eker; Hakan Gurkan
The New Youngest Case of Grange Syndrome with a Novel Biallelic Pathogenic Variant in YY1AP1
Available to Purchase
Taner Karakaya; Ayberk Turkyilmaz; Deniz Eris; Mehtap Kaya; Kupra Oksuz; Meltem Aygul Eryigit; Gizem Gönen
Identification of a Novel IQCE Large Deletion through Copy Number Variant Analysis from Whole-Exome Sequencing Data of a Patient with Postaxial Polydactyly Type A7
Available to Purchase
Faidon-Nikolaos Tilemis; Nikolaos M. Marinakis; Konstantina Kosma; Florentia Fostira; Joanne Traeger-Synodinos
Identification of a Novel Nonsense Variant in the DLL3 Gene Underlying Spondylocostal Dysostosis in a Consanguineous Pakistani Family
Available to Purchase
Feroz Khan; Abida Arshad; Asmat Ullah; Ellen Steenackers; Geert Mortier; Wasim Ahmad; Muhammad Arshad; Sarmir Khan; Amir Hayat; Ikram Khan; Muhammad Asim Khan; Wim Van Hul
Two Patients Diagnosed as Succinate Dehydrogenase Deficiency: Case Report
Available to Purchase
Burcu Civelek Ürey; Ahmet Cevdet Ceylan; Büşranur Çavdarlı; Ayşegül Neşe Çıtak Kurt; Oya Kıreker Köylü; Burak Yürek; Çiğdem Seher Kasapkara
Case Report of Two Siblings Diagnosed with Osteogenesis Imperfecta Type XV with a New Mutation in the WNT1 Gene and Review of the Literature
Available to Purchase
Büşra Eser Çavdartepe; Rojan İpek
Editor's choice
Rania R. Ahmed; Amina M. Medhat; Germine M. Hamdy; Laila K.E. Effat; Mohamed S. Abdel-Hamid; Ghada M.H. Abdel-Salam
Novel Insights from Clinical Practice
DPAGT1-CDG: Report of Two New Pediatric Patients and Brief Review of the Literature
Available to Purchase
Özlem Özsoy; Tayfun Cinleti; Çağatay Günay; Gamze Sarıkaya Uzan; Mehmet Can Yeşilmen; Hanns Lochmüller; Rita Horvath; Uluç Yiş; Yavuz Oktay; Semra Hiz Kurul
Novel Insights from Clinical Practice
Pure Interstitial Trisomy 11q Arising from a Nonrecurrent 11q13.1q22.3 Mosaic Intrachromosomal Duplication in a Patient with Craniofacial Dysmorphism and Genital Anomalies
Available to Purchase
Daniel Martínez Anaya; María del Rocío Juárez-Velázquez; Sinuhé Reyes Ruvalcaba; María del Pilar Navarrete-Meneses; Consuelo Salas Labadía; Esther Lieberman Hernández; Patricia Pérez-Vera
Editor's choice
Clinical Implications of Chromosome 16 Copy Number Variation
Available to Purchase
Emine Ikbal Atli; Sinem Yalcintepe; Engin Atli; Selma Demir; Cisem Mail; Hakan Gurkan
Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance
Available to Purchase
Farooq Ahmad; Ishtiaq Ahmed; Qamre Alam; Tanveer Ahmad; Ammara Khan; Ijaz Ahmad; Muhammad Bilal; Amir Hayat; Amjad Khan; Ahmed Waqas; Misbahuddin M. Rafeeq; Ziaullah M. Sain; Muhammad Umair
