Výsledky vyhledávání - Carole Samango‐Sprouse
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SNP‐based non‐invasive prenatal testing detects sex chromosome aneuploidies with high accuracy Autor Carole Samango‐Sprouse, Milena Banjevic, Allison Ryan, Styrmir Sigurjonsson, Bernhard Zimmermann, Matthew D. Hill, Megan P. Hall, Margaret Westemeyer, Jennifer Saucier, Zachary Demko, Matthew Rabinowitz
Vydáno 2013Artigo -
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XXY (Klinefelter Syndrome): A Pediatric Quantitative Brain Magnetic Resonance Imaging Case-Control Study Autor Jay N. Giedd, Liv Clasen, Gregory L. Wallace, Rhoshel Lenroot, Jason P. Lerch, Elizabeth Wells, Jonathan D. Blumenthal, Jean E. Nelson, Julia W. Tossell, Catherine Stayer, Alan C. Evans, Carole Samango‐Sprouse
Vydáno 2007Artigo -
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Klinefelter syndrome: Expanding the phenotype and identifying new research directions Autor Joe Leigh Simpson, Felix de la Cruz, Ronald S. Swerdloff, Carole Samango‐Sprouse, Niels E. Skakkebæk, John M. Graham, Terry Hassold, Melissa Aylstock, Heino F. L. Meyer‐Bahlburg, Huntington F. Willard, Judith G. Hall, Wael Salameh, Kyle B. Boone, C. Staessen, Dan Geschwind, Jay N. Giedd, Adrian S. Dobs, Alan D. Rogol, Bonnie Brinton, C. Alvin Paulsen
Vydáno 2003Artigo -
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The human inactive X chromosome modulates expression of the active X chromosome Autor Adrianna K. San Roman, Alexander K. Godfrey, Helen Skaletsky, Daniel W. Bellott, Abigail F. Groff, Hannah L. Harris, Laura V. Blanton, Jennifer F. Hughes, Laura G. Brown, Sidaly Phou, Ashley Buscetta, Paul Kruszka, Nicole Banks, Amalia Dutra, Evgenia Pak, Patricia C. Lasutschinkow, Colleen Keen, Shanlee Davis, Nicole Tartaglia, Carole Samango‐Sprouse, Maximilian Muenke, David C. Page
Vydáno 2023Artigo -
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The human Y and inactive X chromosomes similarly modulate autosomal gene expression Autor Adrianna K. San Roman, Helen Skaletsky, Alexander K. Godfrey, Neha V. Bokil, Levi S. Teitz, Isani Singh, Laura V. Blanton, Daniel W. Bellott, Tatyana Pyntikova, Julian Lange, Natalia Koutseva, Jennifer F. Hughes, Laura Brown, Sidaly Phou, Ashley Buscetta, Paul Kruszka, Nicole Banks, Amalia Dutra, Evgenia Pak, Patricia C. Lasutschinkow, Colleen Keen, Shanlee Davis, Angela E. Lin, Nicole Tartaglia, Carole Samango‐Sprouse, Maximilian Muenke, David C. Page
Vydáno 2023Artigo -
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GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases Autor Hellen Lesmann, Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine Marchi, Pilar Caro, Ibrahim M. Abdelrazek, Jean Tori Pantel, Merle ten Hagen, Meow‐Keong Thong, Rifhan Azwani Mazlan, Sok Kun Tae, Tom Kamphans, Wolfgang Meiswinkel, Jingmei Li, Behnam Javanmardi, Alexej Knaus, Annette Uwineza, Cordula Knopp, Tinatin Tkemaladze, Miriam Elbracht, Larissa Mattern, Rami Abou Jamra, Clara Velmans, Vincent Strehlow, Maureen Jacob, Angela Peron, Cristina Dias, Beatriz Nunes, Thainá Vilella, Isabel Furquim Pinheiro, Chong Ae Kim, Maria Isabel Melaragno, Hannah Weiland, Sophia Kaptain, Karolina Chwiałkowska, Mirosław Kwaśniewski, Ramy Saad, Sarah Wiethoff, Himanshu Goel, Clara Sze-Man Tang, Anna Hau, Tahsin Stefan Barakat, Przemysław Panek, Amira Nabil, Julia Suh, Frederik Braun, Israel Gomy, Luisa Averdunk, Ekanem N. Ekure, Gaber Bergant, Borut Peterlin, Claudio Graziano, Nagwa E. A. Gaboon, Moisés Ó. Fiesco-Roa, Alessandro Spinelli, Nina‐Maria Wilpert, Prasit Phowthongkum, Nergis Güzel, Tobias B. Haack, Rana Bitar, Andreas Tzschach, Agustí Rodríguez‐Palmero, Theresa Brunet, Sabine Rudnik–Schöneborn, Silvina Contreras‐Capetillo, Ava Oberlack, Carole Samango‐Sprouse, Teresa Sadeghin, Margaret Olaya, Konrad Platzer, Artem Borovikov, Franziska Schnabel, Lara Heuft, Vera Herrmann, Renske Oegema, Nour Elkhateeb, Sheetal Kumar, Katalin Komlósi, Khoushoua Mohamed, Silvia Kalantari, Fabio Sirchia, Antonio Federico Martínez‐Monseny, Matthias Höller, Louiza Toutouna, Amal Mohamed, Amaia Lasa‐Aranzasti, John A. Sayer, Nadja Ehmke, Magdalena Danyel, Henrike L. Sczakiel, Sarina Schwartzmann, Felix Boschann, Max Zhao, R. Adam, Lara Einicke, Denise Horn, Kee Seang Chew, Choy Chen Kam, Miray Karakoyun
Vydáno 2024Pré-impressão
Vyhledávací nástroje:
Související témata
Medicine
Biology
Gene
Genetics
Chromosome
Internal medicine
Klinefelter syndrome
Aneuploidy
Anatomy
Androgen insensitivity syndrome
Androgen receptor
Cancer
Clinical psychology
Cognition
Endocrinology
Gene expression
Genetic counseling
Genotype
Karyotype
Pediatrics
Phenotype
Pregnancy
Prostate cancer
Psychiatry
Psychology
Surgery
Androgen
Audiology
Autism
Benchmarking