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Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations
Author:
Philibert, Pascal
;
Audran, Francoise
;
Pienkowski, Catherine
Artikel dari
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 94 no. 02 (Jul. 2010)
, page 472-476
Correlation between Hypomethylation of HMOX1 and Cognitive Decline in Patients with Alzheimer’s Disease (abstract only)
Author:
Sung, Hye Youn
;
Choi, Eun Nam
;
Ahn, Jung-Hyuck
Artikel dari
The International Symposium on Social Sciences (TISSS) and Hong Kong International Conference on Education, Psychology and Society (HKICEPS) at Hongkong, December 2013
, page 899
Defining initial strength in clusterless languages in Strict CV
Author:
Kula, Nancy C.
;
Marten, Lutz
Artikel dari
Strength Relations in Phonology
, page 251-284
Detection of Gyrase A Mutation of Porphyromonas Gingivalis gene resistant to Ciprofloxacin by using Polymerase Chain Reaction Technique
Author:
Rieuwpassa, Irene E.
;
Hatta, Mochammad
Artikel dari
Jurnal Kedokteran YARSI vol. 17 no. 01 (Jan. 2009)
, page 11
Detection of Hepatitis B Virus X Gene Mutation from Local Clinical Samples
Author:
Artarini, Anita
;
Jessica, Hanary Geby
;
Kartikasari, Raden Rini
;
Riani, Catur
;
Retnoningrum, Debbie Soefie
Artikel dari
Microbiology Indonesia vol. 10 no. 1 (Mar. 2016)
, page 9-14
Detection of KRAS Mutations and Their Associations with Clinicopathological Features and Survival in Chinese Colorectal Cancer Patients
Author:
Li, Z.
;
Chen, Y.
;
Wang, D.
;
Wang, G.
;
Sadikin-Susilo
Artikel dari
The Journal of International Medical Research vol. 40 no. 04 (Jul. 2012)
, page 1589-1598
Detection of Papua New Guinea Thalassemia Alpha Mutation in Gayo, Sumba, Ternate, and Timika Populations
Author:
Nurfitriani, Risya
;
Abinawanto
;
Noviyanti, Rintis
;
Trianti, Lely
;
Nainggolan, Ita M.
Artikel dari
Makara Seri Sains vol. 18 no. 02 (Jun. 2014)
, page 47-51
Dialogues et Cultures 42 : Le francais et son enseignement ; evolutions et mutations
Author:
[s.n]
Penerbit:
[s.n]
Tahun terbit:
1998
Jenis:
Books
Disease Progression in C9orf72 Mutation Carriers
Author:
Floeter, Mary K.
;
Traynor, Bryan J.
;
Farren, Jennifer
;
Braun, Laura E.
;
Tierney, Michael
;
Wiggs, Edythe A.
;
Tianxia Wu
Artikel dari
Neurology (Official Journal of The American Academy of Neurology) vol. 89 no. 03 (Jul. 2017)
, page 234-241
Divergent effects of the 677C>T mutation of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene on ovarian responsiveness and anti-Müllerian hormone concentrations
Author:
Pavlik, Roman
;
Hecht, Stephanie
;
Ochsenkuhn, Robert
;
Noss, Ulrich
Artikel dari
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 95 no. 07 (Jun. 2011)
, page 2257-2262
Efektivitas penggunaan oseltamivir dalam terapi infeksi influenza H1N1
Author:
DEVIANO, M SANDI
;
DARMAWAN, BUDI
;
Tanzil, Kunadi
(Advisor);
Arieselia, Zita
(Advisor);
Narwati, Benedicta Yulia Tanti
(Examiner)
Penerbit:
Jakarta Utara:
Fakultas Kedokteran Unika Atma Jaya
Tahun terbit:
2011
Jenis:
Theses - Karya Tulis Ilmiah Kedokteran (KTI-FK)
Etiologi Infertilitas pada Pria Akibat dari Mutasi DNA Mitokondria (mtDNA)
Author:
Utami, Sri
Artikel dari
Jurnal Kedokteran MARANATHA vol. 9 no. 1 (Jul. 2009)
, page 87-96
Factor V Leiden and prothrombin gene G20210A mutation and in vitro fertilization: prospective cohort study
Author:
Ricci, Giuseppe
;
Bogatti, Paolo
;
Fischer-Tamaro, Leo
;
Giolo, Elena
Artikel dari
Human Reproduction vol. 26 no. 11 (Nov. 2011)
, page 3068-3077
Father Figures; Genetic Damage and Paternal Age
Author:
[s.n]
Artikel dari
The Economist (http://search.proquest.com/) vol. 404 no. 8799 (Aug. 2012)
, page 64
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
Author:
Fonzo, A. Di
;
Dekker, M.C.J.
;
Montagna, P.
Artikel dari
Neurology (Official Journal of The American Academy of Neurology) vol. 72 no. 03 (Jan. 2009)
, page 240-245
First successful pregnancy in a globozoospermic patient having homozygous mutation in SPATA16
Author:
Karaca, Nilay
;
Yilmaz, Rabiye
;
Kanten, Gulcin E.
;
Kervancioglu, Elif
;
Seyhun, Solakoglu
Artikel dari
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 102 no. 01 (Jul. 2014)
, page 103–107
Galur mutan krisan teleran terhadap fotoperiodisitas.
Author:
Dwimahyani, Ita
Artikel dari
Bulletin Penelitian Universitas Mercu Buana no. 10 (Jul. 2006)
, page 47
Gambaran Polimorfisme Gen CYP2B6 pada Etnis Timor, di Kecamatan Amanuban Selatan, Kabupaten Timor Tengah Selatan, Provinsi Nusa Tenggara Timur, Indonesia
Author:
ALICE, JOSEPHINE
;
Hananta, Linawati
(Advisor);
Ali, Soegianto
(Examiner)
Penerbit:
Jakarta Utara:
Fakultas Kedokteran Unika Atma Jaya
Tahun terbit:
2017
Jenis:
Theses - Karya Tulis Ilmiah Kedokteran (KTI-FK)
Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis
Author:
Bastian, Claire
;
Muller, Jean-Baptiste
;
Lortat-Jacob, Stephen
;
Nihoul-Fekete, Claire
;
Bignon-Topalovic, Joelle
Artikel dari
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 103 no. 05 (May 2015)
, page 1297–1304
Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation
Author:
Trivellin, Giampaolo
;
Daly, Adrian F.
;
Faucz, Fabio R.
;
Bo, Yuan
;
Rostomyan, Liliya
Artikel dari
The New England Journal of Medicine (keterangan: ada di Proquest) vol. 371 no. 25 (Dec. 2014)
, page 2363-2374
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