المؤلفون: Xiaokun Gang, Guixia Wang, You Lv, Zi Yan, Huining Tian, Lin Sun

المصدر: Medicine

مصطلحات موضوعية: Delayed puberty, Male, Urologic Diseases, Pediatrics, medicine.medical_specialty, Receptors, Peptide, Kallmann syndrome, Hormone Replacement Therapy, Urinary system, Mutation, Missense, Nerve Tissue Proteins, Receptors, G-Protein-Coupled, 03 medical and health sciences, Kallmann Syndrome 1, Olfaction Disorders, Young Adult, 0302 clinical medicine, Rare Diseases, Hyposmia, Hypogonadotropic hypogonadism, Cryptorchidism, Exome Sequencing, medicine, Humans, 030212 general & internal medicine, Clinical Case Report, Renal agenesis, Puberty, Delayed, Extracellular Matrix Proteins, business.industry, General Medicine, Micropenis, Exons, medicine.disease, urinary disorders, KAL1, Treatment Outcome, 030220 oncology & carcinogenesis, renal agenesis/dysgenesis, medicine.symptom, Genital Diseases, Male, business, Penis, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53a7316ba1f4e2c36a7c11755772c239Test
https://pubmed.ncbi.nlm.nih.gov/33120852Test

المؤلفون: Yanqiu Hu, Hongshi Yu, Geoff Shaw, Marilyn B. Renfree, Andrew J Pask

المصدر: Biology of Reproduction. 84:595-603

مصطلحات موضوعية: endocrine system, medicine.medical_specialty, Autosome, Gonad, Kallmann syndrome, Cell Biology, General Medicine, Gonadotropin-releasing hormone, Biology, medicine.disease, Cell biology, Anosmin-1, Kallmann Syndrome 1, medicine.anatomical_structure, Endocrinology, Reproductive Medicine, Hypogonadotropic hypogonadism, Internal medicine, medicine, biology.protein, X chromosome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::6ce0dcd1d432a93ea206d8df26d4de84Test
https://doi.org/10.1095/biolreprod.110.087437Test

المؤلفون: Jun-Ping Xing, Wei Xue, Xin-yang Wang, Tie-Jun Zou, Qifei Wu, Kaifa Tang

المصدر: Asian journal of andrology. 11(6)

مصطلحات موضوعية: Adult, Male, China, Adolescent, Kallmann syndrome, Urology, Locus (genetics), Nerve Tissue Proteins, Kallmann Syndrome 1, Exon, Hypogonadotropic hypogonadism, Multiplex polymerase chain reaction, Genotype, Medicine, Humans, Genetics, Extracellular Matrix Proteins, business.industry, Hypogonadism, General Medicine, Kallmann Syndrome, medicine.disease, Molecular analysis, Original Article, business, Gene Deletion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08da926057e33510520f3b37fa9f2108Test
https://pubmed.ncbi.nlm.nih.gov/19734936Test

المؤلفون: Setsuyo Kawakita, Keisuke Nagasaki, Yasuhiro Naiki, Tsutomu Ogata, Naoaki Hori, Shigeru Minowada, Naoko Sato, Tomonobu Hasegawa, Yukihiro Hasegawa, Aki Shimotsuka, Noriyuki Katsumata, Masayo Kagami, Daiichiro Hasegawa, Masato Yokozawa, Katsuhiko Tachibana, Yoshimasa Shishiba, Reiko Horikawa, Toshiaki Tanaka, Toshiyuki Yasuda

المصدر: The Journal of clinical endocrinology and metabolism. 89(3)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pathology, Adolescent, Kallmann syndrome, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, KAL1 gene, DNA Mutational Analysis, Nerve Tissue Proteins, Biochemistry, Contiguous gene syndrome, Anosmin-1, Kallmann Syndrome 1, Endocrinology, Hypogonadotropic hypogonadism, Internal medicine, medicine, Prevalence, Humans, Genetic Predisposition to Disease, Receptor, Fibroblast Growth Factor, Type 1, Child, Family Health, Extracellular Matrix Proteins, biology, Fibroblast growth factor receptor 1, Biochemistry (medical), Receptor Protein-Tyrosine Kinases, Aplasia, Kallmann Syndrome, Middle Aged, medicine.disease, Magnetic Resonance Imaging, Receptors, Fibroblast Growth Factor, Pedigree, Smell, stomatognathic diseases, biology.protein, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d58a6bae738c9bcc2ea8857b39a8ece0Test
https://pubmed.ncbi.nlm.nih.gov/15001591Test

المصدر: Briefings in Functional Genomics.

مصطلحات موضوعية: 0301 basic medicine, biology, KAL1 gene, General Medicine, Computational biology, Biochemistry, Anosmin-1, 03 medical and health sciences, Kallmann Syndrome 1, Gene nomenclature, 030104 developmental biology, Genetics, biology.protein, Human genome, 10. No inequality, Molecular Biology, Gene, Symbol (formal), Nomenclature

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::6961373ed8e7f3c990c890b7d531b734Test