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Lawrence C. Layman results 6 · Newest (Page 1/1, per page 25)
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Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer–Rokitansky–Küster–Hauser (MRKH) syndromeNARA Subscribed
Human Genetics · 2026 · Vol. 145 · Issue 1 · Springer
Dina Kira; Soumia Brakta; Hyung Goo Kim; Jennifer Butler; Lynn P. Chorich; John A. Phillips; Lawrence C. Layman
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Safe vitrification of ovarian tissue samples in sealed cryobagsNARA Subscribed
Cryobiology · 2025 · Vol. 121 · Academic Press
Binnur Eroglu; Lawrence C. Layman; James D. Benson; Adam Z. Higgins; Ali Eroglu
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Rare structural variants, aneuploidies, and mosaicism in individuals with Mullerian aplasia detected by optical genome mappingNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 4 · Springer
Soumia Brakta; Zoe A. Hawkins; Nikhil Sahajpal; Natalie Seman; Dina Kira; Lynn P. Chorich; Hyung-Goo Kim; Hongyan Xu; John A. Phillips; Ravindra Kolhe; Lawrence C. Layman
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Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer–Rokitansky–Küster–Hauser SyndromeNARA Subscribed
Human Genetics · 2021 · Vol. 140 · Issue 4 · Springer
Sasha Mikhael; Sonal Dugar; Madison Morton; Lynn P. Chorich; Kerlene Berwick Tam; Amy C. Lossie; Hyung-Goo Kim; James Knight; Hugh S. Taylor; Souhrid Mukherjee; John A. Capra; John A. Phillips; Michael Friez; Lawrence C. Layman
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An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disabilityNARA Subscribed
Human Genetics · 2016 · Vol. 135 · Issue 7 · Springer
Jonathan D. J. Labonne; Kang-Han Lee; Shigeki Iwase; Il-Keun Kong; Michael P. Diamond; Lawrence C. Layman; Cheol-Hee Kim; Hyung-Goo Kim
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Novel MED12 gene somatic mutations in women from the Southern United States with symptomatic uterine fibroidsNARA Subscribed
Molecular Genetics and Genomics · 2015 · Vol. 290 · Issue 2 · Springer
Sunil K. Halder; Archana Laknaur; Jessica Miller; Lawrence C. Layman; Michael Diamond; Ayman Al-Hendy
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