Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP271122.RAD88KZKWUzUtKQ7zZcXRJhW6nJkw-0wy3PbDYuK3O0lc130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271122.RAD88KZKWUzUtKQ7zZcXRJhW6nJkw-0wy3PbDYuK3O0lc130_provenance.
• NP650472.RAgTlUdx4EAYvccIJdsnM4rY8CSYOO0aT1NCCuAflXY7c130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650472.RAgTlUdx4EAYvccIJdsnM4rY8CSYOO0aT1NCCuAflXY7c130_provenance.
• NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903619.RAVuj91I2VVZz2r-nul1hFdO-bA0GDPA0jF78qky90OYQ130_provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP717021.RA5xzXdXMUCfxQx6YBcbWaQN4ij3J7M-ct-BKPRTvGEdw130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717021.RA5xzXdXMUCfxQx6YBcbWaQN4ij3J7M-ct-BKPRTvGEdw130_provenance.
• NP639767.RA-BHAdQZoCpKXYa5SaC8DE1eRWveepBjDqGhU33NxDdk130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639767.RA-BHAdQZoCpKXYa5SaC8DE1eRWveepBjDqGhU33NxDdk130_provenance.
• NP345371.RAVsbGFPYmS3t1qRi-6SmIJ-hlLBWR-2idtYp6EyirNoo130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345371.RAVsbGFPYmS3t1qRi-6SmIJ-hlLBWR-2idtYp6EyirNoo130_provenance.
• NP811960.RA1ArNJ61qh4PvnNbzKIajXAzIhyagAWiLPQw2wwMqwdA130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811960.RA1ArNJ61qh4PvnNbzKIajXAzIhyagAWiLPQw2wwMqwdA130_provenance.
• NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748914.RAYDl3o4sK2igxPp_wBAz2vry_EHwv4yKQLq8CSZr75JQ130_provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP345378.RAA4zzvY_Bdd8Xvf4xUf99sfZkIpDST-zkQyERJX2bxx0130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345378.RAA4zzvY_Bdd8Xvf4xUf99sfZkIpDST-zkQyERJX2bxx0130_provenance.
• NP475372.RADoQvMIULdVZER8CiMIPvUUsn-nmlNRFT_jUJzv_H5sA130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475372.RADoQvMIULdVZER8CiMIPvUUsn-nmlNRFT_jUJzv_H5sA130_provenance.
• NP748854.RAnk5pP_bb8WXpIjcXXsdIihVrJqE1mBwCvadu9lDbgr0130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748854.RAnk5pP_bb8WXpIjcXXsdIihVrJqE1mBwCvadu9lDbgr0130_provenance.
• NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_provenance.
• NP475365.RAeThj7jZQRtiZ5n6IjlFD7b6ubN30_rGAoGNusxOtVb0130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475365.RAeThj7jZQRtiZ5n6IjlFD7b6ubN30_rGAoGNusxOtVb0130_provenance.
• NP475367.RAcErD211W4H6aSgUiJRoOppi-Z9oPXp2J1_IHsFwzbS0130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475367.RAcErD211W4H6aSgUiJRoOppi-Z9oPXp2J1_IHsFwzbS0130_provenance.
• NP475368.RAc5jokNTZkKHdeQd90_rEybWI5OFchNp7F7Mh7Qeb6tE130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475368.RAc5jokNTZkKHdeQd90_rEybWI5OFchNp7F7Mh7Qeb6tE130_provenance.
• NP475374.RAfq5ODpzJpUA8HkTDbvHamZaSm1goo5abrVPvqvFASpY130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475374.RAfq5ODpzJpUA8HkTDbvHamZaSm1goo5abrVPvqvFASpY130_provenance.
• NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475376.RAa7AT60nlB63dVVYSHTMaOlDYNE4ytou83S-wrVGTNuI130_provenance.
• NP475377.RAebqljrIHp56XcgvkaQDk9hDXmr21bim3Jkk-6KaWX0c130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475377.RAebqljrIHp56XcgvkaQDk9hDXmr21bim3Jkk-6KaWX0c130_provenance.
• NP475378.RAXBt96xxCB4-YISdDc4j_jYV5m1VkV5v2Zdkapo0mNDs130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475378.RAXBt96xxCB4-YISdDc4j_jYV5m1VkV5v2Zdkapo0mNDs130_provenance.
• NP345389.RANdt7MtCXMBwssRBI7irVYZ8JoJ79bKH6gsgF-AgNqvE130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345389.RANdt7MtCXMBwssRBI7irVYZ8JoJ79bKH6gsgF-AgNqvE130_provenance.
• NP475370.RAHTUN29N2ua_TPyQKz87m47XdHG7vBj6TPmcYluk5D0s130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475370.RAHTUN29N2ua_TPyQKz87m47XdHG7vBj6TPmcYluk5D0s130_provenance.
• NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
• NP475379.RAOkq_RDXr7vjTNA2FFtzVyDMZo7z9mc7MuiruYxgfoTc130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475379.RAOkq_RDXr7vjTNA2FFtzVyDMZo7z9mc7MuiruYxgfoTc130_provenance.
• NP748852.RA6AdrlRaQfJ_bxKyT-RYi4q0RxbpJkpvNhE5c-aYpFmw130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748852.RA6AdrlRaQfJ_bxKyT-RYi4q0RxbpJkpvNhE5c-aYpFmw130_provenance.
• NP748855.RAwdvr0l9NSvyWuJhNBxCpnilr3NqdN40ylVzOe_58NCM130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748855.RAwdvr0l9NSvyWuJhNBxCpnilr3NqdN40ylVzOe_58NCM130_provenance.
• NP748856.RA3qneasngaxf6wQlDLU8DmJpGMOID3Kva5s532X7iVFg130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748856.RA3qneasngaxf6wQlDLU8DmJpGMOID3Kva5s532X7iVFg130_provenance.
• NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_provenance.
• NP748909.RA6eqqvVZdTiqTSbAR6GfvMN5Vyreq6_Wm4hlc0iUCt9M130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748909.RA6eqqvVZdTiqTSbAR6GfvMN5Vyreq6_Wm4hlc0iUCt9M130_provenance.
• NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_provenance.
• NP475369.RA-FD_6pjeiNzoiHnqP9-7COdj7J9r8411q31a3dYqN2o130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475369.RA-FD_6pjeiNzoiHnqP9-7COdj7J9r8411q31a3dYqN2o130_provenance.
• NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475371.RA2ppN4UNRQecfg1DzPYE32mLwGiZIto-qXzwNTx4dPHI130_provenance.
• NP475375.RA-6ZVtfCmp2LYHk7iQrQCD8CEv7HTGPzyIjNPdxs0oWk130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475375.RA-6ZVtfCmp2LYHk7iQrQCD8CEv7HTGPzyIjNPdxs0oWk130_provenance.