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Results for
""Chromosomes, Human, Pair 7""[mesh_terms]

20 Results

Searching titles within these results

New genetic insights in familial hyperaldosteronism.

Richard V Jackson, Anthony Lafferty, David J Torpy, Constantine Stratakis

Annals of the New York Academy of Sciences 2002;970():77-88

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Abstract

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.

Kinga Kozma, Marius Bembea, Claudia M Jurca, Mihai Ioana, Ioana Streață, Simona Ş Şoşoi, Andrei Pirvu, Codruța D Petchesi, Ariana Szilágyi, Cristian N Sava, Alexandru Jurca, Anikó Ujfalusi, Zsuzsanna Szűcs, Katalin Szakszon

Genes 2022;12(11):1674

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A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.

Jie Hu, Sofia Shekhter-Levin, Peter H Shaw, Carolyn Bay, Sally Kochmar, Urvashi Surti

Cancer genetics and cytogenetics 2005;156(1):62-7

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Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability.

Marlene Lorgen-Ritchie, Alison D Murray, Anne C Ferguson-Smith, Marcus Richards, Graham W Horgan, Louise H Phillips, Gwen Hoad, Ishbel Gall, Kristina Harrison, Geraldine McNeill, Mitsuteru Ito, Paul Haggarty

PloS one 2019;14(2):e0211799

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A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani family.

Amir Hayat, Atif Ahmad Khan, Abdur Rauf, Saad Ullah Khan, Shabir Hussain, Asmat Ullah, Wasim Ahmad, Sulaiman Shams, Bushra Khan

Clinical dysmorphology 2020;29(1):17-23

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McLeod syndrome: a neurohaematological disorder.

H H Jung, A Danek, B M Frey

Vox sanguinis 2007;93(2):112-21

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Recurrent deletions of IKZF1 in pediatric acute myeloid leukemia.

Jasmijn D E de Rooij, Eva Beuling, Marry M van den Heuvel-Eibrink, Askar Obulkasim, André Baruchel, Jan Trka, Dirk Reinhardt, Edwin Sonneveld, Brenda E S Gibson, Rob Pieters, Martin Zimmermann, C Michel Zwaan, Maarten Fornerod

Haematologica 2016;100(9):1151-9

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JAZF1/JJAZ1 gene fusion in endometrial stromal sarcomas: molecular analysis by reverse transcriptase-polymerase chain reaction optimized for paraffin-embedded tissue.

Andelko Hrzenjak, Farid Moinfar, Fattaneh A Tavassoli, Bettina Strohmeier, Marie-Luise Kremser, Kurt Zatloukal, Helmut Denk

The Journal of molecular diagnostics : JMD 2005;7(3):388-95

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Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3.

A V Postma, C R Bezzina, J F de Vries, A A Wilde, A F Moorman, M M Mannens

Human genetics 2000;106(6):614-9

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A review of the Colton blood group system.

G R Halverson, T Peyrard

Immunohematology 2010;26(1):22-6

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Genetic association of gastric cancer with miRNA clusters including the cancer-related genes MIR29, MIR25, MIR93 and MIR106: results from the EPIC-EURGAST study.

Yolanda Espinosa-Parrilla, Xavier Muñoz, Catalina Bonet, Nadia Garcia, Adoración Venceslá, Nikos Yiannakouris, Alessio Naccarati, Sabina Sieri, Salvatore Panico, José M Huerta, Aurelio Barricarte, Virginia Menéndez, Emilio Sánchez-Cantalejo, Miren Dorronsoro, Paul Brennan, Talita Duarte-Salles, H B As Bueno-de-Mesquita, Elisabete Weiderpass, Eiliv Lund, Françoise Clavel-Chapelon, Marie-Christine Boutron-Ruault, Antoine Racine, Mattijs E Numans, Rosario Tumino, Federico Canzian, Daniele Campa, Malin Sund, Mattias Johansson, Bodil Ohlsson, Björn Lindkvist, Kim Overvad, Anne Tjønneland, Domenico Palli, Ruth C Travis, Kay-Tee Khaw, Nick Wareham, Heiner Boeing, Gabriella Nesi, Elio Riboli, Carlos A Gonzalez, Núria Sala

International journal of cancer 2014;135(9):2065-76

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Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.

H S Kuehn, B Boisson, C Cunningham-Rundles, J Reichenbach, A Stray-Pedersen, E W Gelfand, P Maffucci, K R Pierce, J K Abbott, K V Voelkerding, S T South, N H Augustine, J S Bush, W K Dolen, B B Wray, Y Itan, A Cobat, H S Sorte, S Ganesan, S Prader, T B Martins, M G Lawrence, J S Orange, K R Calvo, J E Niemela, J-L Casanova, T A Fleisher, H R Hill, A Kumánovics, M E Conley, S D Rosenzweig

The New England journal of medicine 2016;374(11):1032-1043

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Therapy-related myelodysplastic syndrome after eradication of acute promyelocytic leukemia: cytogenetic and molecular features.

W Y Au, C C Lam, E S Ma, C Man, T Wan, Y L Kwong

Human pathology 2001;32(1):126-9

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Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.

Marilyn C Cornelis, Keri L Monda, Kai Yu, Nina Paynter, Elizabeth M Azzato, Siiri N Bennett, Sonja I Berndt, Eric Boerwinkle, Stephen Chanock, Nilanjan Chatterjee, David Couper, Gary Curhan, Gerardo Heiss, Frank B Hu, David J Hunter, Kevin Jacobs, Majken K Jensen, Peter Kraft, Maria Teresa Landi, Jennifer A Nettleton, Mark P Purdue, Preetha Rajaraman, Eric B Rimm, Lynda M Rose, Nathaniel Rothman, Debra Silverman, Rachael Stolzenberg-Solomon, Amy Subar, Meredith Yeager, Daniel I Chasman, Rob M van Dam, Neil E Caporaso

PLoS genetics 2011;7(4):e1002033

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Childhood myelodysplastic syndrome.

Tathagata Chatterjee, V P Choudhry

Indian journal of pediatrics 2014;80(9):764-71

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Results: 1 – 15 / 20

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Results for ""Chromosomes, Human, Pair 7""[mesh_terms]

New genetic insights in familial hyperaldosteronism.

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.

A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.

Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability.

A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani family.

McLeod syndrome: a neurohaematological disorder.

Recurrent deletions of IKZF1 in pediatric acute myeloid leukemia.

JAZF1/JJAZ1 gene fusion in endometrial stromal sarcomas: molecular analysis by reverse transcriptase-polymerase chain reaction optimized for paraffin-embedded tissue.

Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3.

A review of the Colton blood group system.

Genetic association of gastric cancer with miRNA clusters including the cancer-related genes MIR29, MIR25, MIR93 and MIR106: results from the EPIC-EURGAST study.

Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.

Therapy-related myelodysplastic syndrome after eradication of acute promyelocytic leukemia: cytogenetic and molecular features.

Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.

Childhood myelodysplastic syndrome.

Results for
""Chromosomes, Human, Pair 7""[mesh_terms]