المؤلفون: Souissi, Asmahane^{Aff4, Aff5, Aff6}, Toukabri, Nourchène^{Aff7, Aff3}, Chelly, Ines^{Aff8, Aff9, Aff10}, Laaroussi, Nadia^Aff11, Charfeddine, Cherine^Aff12, Hafsi, Wissem^{Aff14, Aff15}, Abdelhak, Sonia^Aff11, Boubaker, Samir^{Aff16, Aff13}, Mokni, Mourad^Aff6

المساهمون: Smoller, Bruce, editor^Aff1, Bagherani, Nooshin, editor^Aff2

المصدر: Atlas of Dermatology, Dermatopathology and Venereology : Cutaneous Anatomy, Biology and Inherited Disorders and General Dermatologic Concepts. :517-546

المؤلفون: Pope, Elena^Aff3, Deodhare, Namita^Aff4, Lara-Corrales, Irene^Aff3

المساهمون: Smoller, Bruce, editor^Aff1, Bagherani, Nooshin, editor^Aff2

المصدر: Atlas of Dermatology, Dermatopathology and Venereology : Cutaneous Anatomy, Biology and Inherited Disorders and General Dermatologic Concepts. :585-633

المؤلفون: Gondokaryono, Srie Prihianti^{Aff4, Aff5}, Diana, Inne Arline^{Aff4, Aff5}, Effendi, Raden Mohamad Rendy Ariezal^{Aff4, Aff5}, Dwiyana, Reiva Farah^{Aff4, Aff5}

المساهمون: Norman, Robert A., Series Editor^Aff1, Arcangeli, Fabio, editor^Aff2, Lotti, Torello M., editor^Aff3

المصدر: Clinical Cases in Neonatal and Infant Dermatology. :111-114

المؤلفون: Suzanne Xu, BS, Katharine T. Ellis, BS, Simon F. Roy, MD, Margaret S. Johnston, MD, Amanda E. Zubek, MD, PhD

المصدر: JAAD Case Reports, Vol 31, Iss , Pp 59-61 (2023)

مصطلحات موضوعية: Blaschko’s lines, focal dermal hypoplasia, Goltz syndrome, X-linked dominant disorder, Dermatology, RL1-803

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S235251262200488X; https://doaj.org/toc/2352-5126

URL الوصول: https://doaj.org/article/bf633d12027f411da485d0d359aa10da

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المؤلفون: Fackler, Nathan, Zachary, Cameron, Kim, Dong Joo, Smith, Janellen, Sarpa, Hege Grande

المصدر: JAAD case reports. 4(10)

مصطلحات موضوعية: CHILD syndrome, CHILD, Congenital hemidysplasia with ichthyosiform nevus and limb defects, CNS, central nervous system, NSDHL, NAD(P) dependent steroid dehydrogenase-like gene, SHH, sonic hedgehog hormone, X-linked dominant, congenital hemidysplasia with ichthyosiform nevus and limb defects syndrome, congenital nevus, erythema, genodermatosis, hemidysplasia, limb defect, scaling, CHILD, Congenital hemidysplasia with ichthyosiform nevus and limb defects, CNS, central nervous system, NSDHL, NAD(P) dependent steroid dehydrogenase-like gene, SHH, sonic hedgehog hormone

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/8w34q4cp

المؤلفون: Kudo, Yoshiki^Aff4

المساهمون: Konishi, Ikuo, Series Editor^Aff1, Katabuchi, Hidetaka, Series Editor^Aff2, Masuzaki, Hideaki, editor^Aff3

المصدر: Fetal Morph Functional Diagnosis. :71-80

المؤلفون: Tian Xu, Xiaohui Tao, Zhenlin Zhang, Hua Yue

المصدر: Frontiers in Endocrinology, Vol 13 (2022)

مصطلحات موضوعية: X-linked dominant hypophosphatemia, PHEX, fibroblast growth factor 23, clinical features, gene mutation, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fendo.2022.956646/full; https://doaj.org/toc/1664-2392

URL الوصول: https://doaj.org/article/75a2ed7300914b2ea7375539d3df0708

المؤلفون: Maria Mansouri, Fatima Zohra Bouzid, Said Amal, Oufae Hocar, Nissrine Aboussair

المصدر: Indian Journal of Dermatology, Vol 68, Iss 1, Pp 122-122 (2023)

مصطلحات موضوعية: ectodermal manifestations, focal dermal hypoplasia, porcn gene, x-linked dominant disease, Dermatology, RL1-803

وصف الملف: electronic resource

Relation: http://www.e-ijd.org/article.asp?issn=0019-5154;year=2023;volume=68;issue=1;spage=122;epage=122;aulast=Mansouri; https://doaj.org/toc/0019-5154; https://doaj.org/toc/1998-3611

URL الوصول: https://doaj.org/article/776a9cc7aeb24dbcb8ff4bc8e926e297

المؤلفون: El-Darouti, Mohammad Ali^Aff3, Al-Ali, Faiza Mohamed^Aff4

المساهمون: El-Darouti, Mohammad Ali^Aff1, Al-Ali, Faiza Mohamed^Aff2

المصدر: Challenging Cases in Dermatology Volume 2 : Advanced Diagnoses and Management Tactics. :75-82