المؤلفون: van Heerwaarde AA, Klomberg RCW, van Ravenswaaij-Arts CMA, Ploos van Amstel HK, A Toekoen, Jessurun F, Garg A, van der Kaay DCM

المصدر: Yearbook of Paediatric Endocrinology.

مصطلحات موضوعية: General Economics, Econometrics and Finance

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::6915510d6caffaac984969fb1bcd6529
https://doi.org/10.1530/ey.19.13.12

المؤلفون: Pieter H. Reitsma, Ploos van Amstel Hk, Ernest Briët, Jeroen Eikenboom

المصدر: Thrombosis and Haemostasis. 68:448-454

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Messenger RNA, biology, Nonsense mutation, Nucleic acid sequence, Hematology, Molecular biology, Stop codon, Exon, Von Willebrand factor, hemic and lymphatic diseases, biology.protein, Missense mutation, Gene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::685d8b983e3df785753293082b94a172
https://doi.org/10.1055/s-0038-1646295

المؤلفون: van der Logt Cp, Pieter H. Reitsma, Rogier M. Bertina, Ploos van Amstel Hk

المصدر: Biochemistry. 29:7853-7861

مصطلحات موضوعية: Pseudogene, Molecular Sequence Data, Biochemistry, Protein S, Homology (biology), Exon, Humans, Amino Acid Sequence, RNA, Messenger, Gene, Glycoproteins, Genetics, Genomic Library, Splice site mutation, Base Sequence, biology, Alternative splicing, Intron, DNA, Exons, Biological Evolution, Molecular biology, Introns, Multigene Family, biology.protein, Pseudogenes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e54ac235a61380eefa58514279dc38c6
https://doi.org/10.1021/bi00486a011

المؤلفون: Voorhuis M, Onland-Moret NC, Fauser BC, Ploos van Amstel HK, van der Schouw YT, Broekmans FJ

المصدر: Human Reproduction; Feb2013, Vol. 28 Issue 2, p496-501, 6p

المؤلفون: Pieter H. Reitsma, K. Hamulyak, Ploos van Amstel Hk, P. M. Mannucci, de Die-Smulders Ce, Rogier M. Bertina

المصدر: Thrombosis and Haemostasis. 62:897-901

مصطلحات موضوعية: Genetics, Mutation, biology, Pseudogene, Hematology, medicine.disease, medicine.disease_cause, Molecular biology, Protein S, Restriction site, Centimorgan, Restriction enzyme, biology.protein, medicine, Protein S deficiency, Gene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::6e8fb987c5c6f024d580acd6c61e8f8c
https://doi.org/10.1055/s-0038-1651024

المؤلفون: Ploos van Amstel, HK, Huisman, MV, Reitsma, PH, Wouter ten Cate, J, Bertina, RM

المصدر: Blood; February 1989, Vol. 73 Issue: 2 p479-483, 5p

المؤلفون: Bertina, RM, Ploos van Amstel, HK, van Wijngaarden, A, Coenen, J, Leemhuis, MP, Deutz-Terlouw, PP, van der Linden, IK, Reitsma, PH

المصدر: Blood; August 1990, Vol. 76 Issue: 3 p538-548, 11p

المؤلفون: Hostra, RMW, Landsvater, R M, Ceccherini, I, Stulp, R P, Stelwagen, T, Luo, Y, Pasini, B, Hoppener, JWM, Ploos van Amstel, HK, Romeo, G, Lips, CJM, Buys, CHCM

المصدر: Endocrinologist; May1994, Vol. 4 Issue 3, p225-225, 1p

عنوان ترانسليتريتد: Ernstige hypodontie: meer dan alleen ontbrekende gebitselementen?

المؤلفون: Ross JN, Ruigrok LC, Fennis WMM, Cune MS, Rosenberg AJWP, van Nunen AB, Créton MA, Ploos van Amstel HK, van den Boogaard MJJH

المصدر: Nederlands tijdschrift voor tandheelkunde [Ned Tijdschr Tandheelkd] 2023 Jun; Vol. 130 (6), pp. 277-286.

نوع المنشور: Case Reports; English Abstract; Journal Article

بيانات الدورية: Publisher: Prelum Country of Publication: Netherlands NLM ID: 0400771 Publication Model: Print Cited Medium: Print ISSN: 0028-2200 (Print) Linking ISSN: 00282200 NLM ISO Abbreviation: Ned Tijdschr Tandheelkd

مواضيع طبية MeSH: Anodontia*/pathology , Tooth*, Humans ; Odontogenesis

المؤلفون: Ross JN; Department of Oral-Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Center Utrecht, Utrecht, the Netherlands., Ruigrok LC; Department of Fixed and Removable, Prosthodontics and Biomaterials, Center for Dentistry and Oral Hygiene, University Medical Center Groningen, Groningen, the Netherlands., Fennis WMM; Department of Oral-Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Center Utrecht, Utrecht, the Netherlands., Cune MS; Department of Oral-Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Center Utrecht, Utrecht, the Netherlands.; Department of Fixed and Removable, Prosthodontics and Biomaterials, Center for Dentistry and Oral Hygiene, University Medical Center Groningen, Groningen, the Netherlands.; Department of Oral-Maxillofacial Surgery, Prosthodontics and Special Dental Care, St. Antonius Hospital Nieuwegein, Nieuwegein, the Netherlands., Rosenberg AJWP; Department of Oral-Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Center Utrecht, Utrecht, the Netherlands., van Nunen AB; Department of Internal Medicine and Gastroenterology, Zuyderland Medical Center, Heerlen, the Netherlands., Créton MA; Department of Oral-Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Center Utrecht, Utrecht, the Netherlands.; Department of Dentistry, Radboud Institute for Health Sciences, Section of Orthodontics and Craniofacial Biology, Radboud university medical center, Nijmegen, the Netherlands., Ploos van Amstel HK; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands., van den Boogaard MJH; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.

المصدر: Oral diseases [Oral Dis] 2023 Jan; Vol. 29 (1), pp. 300-307. Date of Electronic Publication: 2021 Jul 14.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 9508565 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1601-0825 (Electronic) Linking ISSN: 1354523X NLM ISO Abbreviation: Oral Dis

مواضيع طبية MeSH: Anodontia*/genetics, Humans ; Case-Control Studies ; Mutation ; Wnt Signaling Pathway/genetics