PubMed for id: 138005

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37569761,36803361,35844343,35057802,33104226,32926563,32070177,31776469,31191205,31176769,30406119,28900819,28395085,25014561,24798461,24780443,24462883,24059671,23895774,23812912,23453666,23266643,23123320,22528406,20138017,20020466,19763616,19635726,19520280,19450439,18851904,18764972,18197200,17621486,17159518,16440880,15216542,12493053,12405447,12269734,11194944,10963101,10029266,8777806,8725783,8556302,8151082,8107989,7826709,7747786,2246489,1953417,1456296,914974,38136965,37945024,37592902,37580113,37466007,37372388,37186309,37078131,36999555,36879246,36843332,36757831,36747105,36728747,36709937,36553631,36444493,36345169,36321570,36232804,36074901,35965362,35881308,35861646,35708058,35599435,35451546,35119035,34873726,34800363,34706719,34674206,34652576,34621002,34611884,34562182,34519148,34400773,34325981,34210538,34037727,33768696,33750440,33728854,33722742,33588214,33413009,33271615,33186761,33179233,33106617,32972427,32896090,32798076,32705776,32531460,32482919,32415730,32335881,32312822,32275884,32169460,32031333,31990480,31925597,31796684,31727177,31627234,31562959,31511512,31207318,31079899,31064326,30961548,30945334,30808755,30612693,30595068,30268123,30142437,30121372,30032983,30005813,29966135,29907476,29902589,29883675,29858378,29858110,29549119,29427453,29421787,29410512,29371155,29305346,29175559,29136354,28851325,28781028,28377321,28187749,28160395,27940755,27852030,27764520,27511161,27502409,27399968,27250695,27108886,27061120,26926398,26916325,26852512,26349186,26238961,26235985,26174511,26114344,25979662,25804024,25714560,25510707,25230004,25053001,24989451,24715670,24665034,24658322,24458657,24228726,24194475,24193349,23965854,23963297,23820807,23817307,23704079,23643445,23637025,23622185,23523603,23403231,23296430,23142271,23125460,23065275,23021068,22821890,22768674,22686558,22610665,22564885,22505049,22450339,22354677,22140031,22129046,22036171,21990267,21946454,21834622,21744487,21488007,21337689,21225925,21211919,21204234,20967465,20949508,20817921,20729831,20512159,20395089,20219702,19924563,19856229,19806373,19760655,19594370,19578037,19380077,19277761,19215039,18757045,18642369,18642362,18546282,18445675,18286822,18195110,18019372,17764080,17634419,17328266,17159513,17152069,16972175,16857757,16824814,16650080,16470698,16418593,16417876,16411218,16272165,16190882,16088922,16088863,15967614,15904436,15812461,15810008,15662685,15549153,15389894,15372524,15309625,15216543,15216407,15057127,14738943,14708106,14634983,12794702,12504316,12453509,12088311,11754060,11669356,11576410,11533803,11438988,11222639,11173961,11074119,10893662,10818153,10797421,10756349,10654660,10448799,10353782,10323316,10206234,9926316,9832558,9810564,9805990,9727748,9689623,9610803,9555580,9450876,9300653,9266556,9157201,8983728,8836504,8648535,8368261,8327066,8213924,7985573,7977460,7880337,7573131,7570585,3400727,3344762,3055985,2956282,2706841,2453812,2279363,1887836,1442884,1287564,38498110,38480026,38303731,38215144,38188845,38179413,38162156,37994142,37794925,37676105,37523070,37371788,37181183,37105048,37063680,36876345,36640836,36568277,36551411,36281281,35868222,35307464,35130247,35115485,34765486,34702808,34557665,34250854,34081427,34006278,33717247,33374895,33029437,32627805,32563254,32549991,32477580,32257294,32018937,31972069,31917496,31687265,31321300,30800538,30799663,30774715,30573562,30546152,30445565,29944857,29938437,29843537,29801921,29664449,29659433,28887793,28706620,28680612,28638259,28374019,28074379,27978593,27909566,27638326,27625832,27620364,27195044,27161462,27159668,27141501,27081522,27081496,27075009,26848311,26808679,26793073,26584551,26398942,26156442,26000327,25895913,24985752,24856766,24678945,24592343,23705081,23598830,23565482,23317051,23233151,22992533,22975854,22914838,22884749,22855961,22801186,22423107,22330852,22246904,22044576,22002442,21950800,21932181,21815259,21741276,21555052,21533562,20576785,20301502,20158397,19919787,19738385,19606480,19480336,19182162,18618999,18287574,18250116,17957045,17698520,17593378,17351359,17351351,17207597,16636621,16627861,16531728,16477654,16338878,16265999,16237361,15862859,15679191,15465400,15365720,15094649,15030912,14762712,14533067,12808501,12599524,12533323,12378571,12373681,11878585,11865707,11848116,11770884,11676163,11587882,11430871,11321983,11301227,11164829,11113917,11105628,10720912,10670895,10587040,10532171,10502009,10415403,10363323,9805987,9710036,9569260,9381566,9354804[uid]

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A Variant in TBCD Associated with Motoneuronopathy and Corpus Callosum Hypoplasia: A Case Report.

Caputo M, Martinelli I, Fini N, Gianferrari G, Simonini C, Trovato R, Santorelli FM, Tessa A, Mandrioli J, Zucchi E. Caputo M, et al. Int J Mol Sci. 2023 Aug 3;24(15):12386. doi: 10.3390/ijms241512386. Int J Mol Sci. 2023. PMID: 37569761 Free PMC article.

Spinal muscular atrophy with hypoplasia of the corpus callosum: a case report.

Zhu X, Li H, Hu C, Wu M, Zhou S, Wang Y, Li W. Zhu X, et al. BMC Neurol. 2023 Feb 18;23(1):77. doi: 10.1186/s12883-023-03121-w. BMC Neurol. 2023. PMID: 36803361 Free PMC article.

A Case of Ophthalmoplegia, Hypotonia, and Developmental Delay in the Setting of Corpus Callosum Hypoplasia.

Kim EY, Trejo S Jr, Nguyen EB, Malwane MI, Cucalón-Calderón JR. Kim EY, et al. Cureus. 2022 Jun 14;14(6):e25930. doi: 10.7759/cureus.25930. eCollection 2022 Jun. Cureus. 2022. PMID: 35844343 Free PMC article.

Holoprosencephalia, hypoplasia of corpus callosum and cerebral heterotopia in a male belted Galloway heifer with adipsia.

Nessler J, Wunderlich C, Eikelberg D, Beineke A, Raue J, Runge M, Tipold A, Ganter M, Rehage J. Nessler J, et al. BMC Vet Res. 2022 Jan 20;18(1):51. doi: 10.1186/s12917-022-03152-4. BMC Vet Res. 2022. PMID: 35057802 Free PMC article.

Familial Exudative Vitreoretinopathy With Neurodevelopmental Delay and Hypoplasia of the Corpus Callosum.

Amorelli GM, Barresi C, Ji MH, Orazi L, Molle F, Lepore D. Amorelli GM, et al. Ophthalmic Surg Lasers Imaging Retina. 2020 Oct 1;51(10):588-591. doi: 10.3928/23258160-20201005-07. Ophthalmic Surg Lasers Imaging Retina. 2020. PMID: 33104226

A novel NFIA gene nonsense mutation in a Chinese patient with macrocephaly, corpus callosum hypoplasia, developmental delay, and dysmorphic features.

Zhang Y, Lin CM, Zheng XL, Abuduxikuer K. Zhang Y, et al. Mol Genet Genomic Med. 2020 Nov;8(11):e1492. doi: 10.1002/mgg3.1492. Epub 2020 Sep 14. Mol Genet Genomic Med. 2020. PMID: 32926563 Free PMC article.

Hypoplasia of the Corpus Callosum: A Single Center Experience and a Concise Literature Review.

D'Ambrosio V, Boccherini C, Manganaro L, Panici PB, Cellitti R, Vena F, Pajno C, Corno S, Brunelli R, Giancotti A. D'Ambrosio V, et al. Fetal Pediatr Pathol. 2021 Dec;40(6):626-637. doi: 10.1080/15513815.2020.1723148. Epub 2020 Feb 18. Fetal Pediatr Pathol. 2021. PMID: 32070177 Review.

De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy.

Nabais Sá MJ, Venselaar H, Wiel L, Trimouille A, Lasseaux E, Naudion S, Lacombe D, Piton A, Vincent-Delorme C, Zweier C, Reis A, Trollmann R, Ruiz A, Gabau E, Vetro A, Guerrini R, Bakhtiari S, Kruer MC, Amor DJ, Cooper MS, Bijlsma EK, Barakat TS, van Dooren MF, van Slegtenhorst M, Pfundt R, Gilissen C, Willemsen MA, de Vries BBA, de Brouwer APM, Koolen DA. Nabais Sá MJ, et al. Genet Med. 2020 Apr;22(4):797-802. doi: 10.1038/s41436-019-0703-y. Epub 2019 Nov 28. Genet Med. 2020. PMID: 31776469 Free article.

1q42.12q42.2 Deletion in a Child with Midline Defects and Hypoplasia of the Corpus Callosum.

Radha Rama Devi A, Ganapathy A, Mannan AU, Sabharanjak S, Naushad SM. Radha Rama Devi A, et al. Mol Syndromol. 2019 May;10(3):161-166. doi: 10.1159/000496079. Epub 2019 Jan 16. Mol Syndromol. 2019. PMID: 31191205 Free PMC article.

Novel BRPF1 mutation in a boy with intellectual disability, coloboma, facial nerve palsy and hypoplasia of the corpus callosum.

Demeulenaere S, Beysen D, De Veuster I, Reyniers E, Kooy F, Meuwissen M. Demeulenaere S, et al. Eur J Med Genet. 2019 Aug;62(8):103691. doi: 10.1016/j.ejmg.2019.103691. Epub 2019 Jun 6. Eur J Med Genet. 2019. PMID: 31176769

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