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List of works by Lucina Bobadilla-Morales

A familial Xp+ chromosome, dup (Xq26.3-->qter).

scientific article

A translocation t(5;15)(q15;q11-13) infant case with acute lymphoblastic leukemia and literature review: prognosis implications.

scientific article published on July 2012

Aneuploidy identification in pre-B acute lymphoblastic leukemia patients at diagnosis by Multiplex Ligation-dependent Probe Amplification (MLPA).

scientific article published in June 2017

Angelman syndrome and thyroid dysfunction

scientific article published on 01 January 2012

Aplasia Cutis Congenita of the Scalp in a Female Infant With Anophthalmia/Microphthalmia-Esophageal Atresia Syndrome Negative forSOX2Mutation

Associated congenital anomalies in infants with isolated gastroschisis: A single-institutional experience.

scientific article published on 14 October 2015

Cell cycle and centromere FISH studies in premature centromere division

scientific article

Chromosome instability induced in vitro with mitomycin C in five Seckel syndrome patients.

scientific article published in December 2003

Cleft lip and/or palate in two cases of 46,X,i(Xq) Turner syndrome

article

Co-occurrence of hemiscrotal agenesis with cutis marmorata telangiectatica congenita and hydronephrosis affecting the same side of the body.

scientific article

Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy.

scientific article published on 22 November 2016

Confirmation of the macroblepharon, ectropion, hypertelorism, and macrostomia syndrome

Curcumin potentiates the effect of chemotherapy against acute lymphoblastic leukemia cells via downregulation of NF-κB.

scientific article published on 30 September 2016

Cytotoxic effect of curcumin on Giardia lamblia trophozoites.

scientific article published on 5 May 2006

DNA damage in mouse lymphocytes exposed to curcumin and copper

scholarly article by Patricia Urbina-Cano et al published December 2006 in Journal of Applied Genetics

Descriptive study of the complete blood count in newborn infants with Down syndrome.

scientific article published on 7 February 2017

Development of an effective and rapid qPCR for identifying human ChREBPα/β isoforms in hepatic and adipose tissues

scientific article published on 27 February 2019

Dysgnathia complex sine holoprosencephaly nor synotia: a case report and discussion of its nosology

scientific article published on January 1, 2013

Floating-Harbor syndrome. A neuropsychological approach

scientific article published on 01 January 1996

GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome.

scientific article published on 8 March 2017

Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects. A new syndrome?

scientific article published on 01 January 1996

Holoprosencephaly, hypertelorism, and ectrodactyly in a boy with an apparently balanced de novo t(2;4)(q14.2;q35)

scientific article published on 01 February 2000

New amino acid changes in drug resistance sites and HBsAg in hepatitis B virus genotype H.

scientific article published on 2 March 2015

Oblique facial clefts in Johanson-Blizzard syndrome

Pediatric donor cell leukemia after allogeneic hematopoietic stem cell transplantation in AML patient from related donor

scientific article

Prevalence and risk factors for gastroschisis in a public hospital from west México

Prevalence of orofacial clefts and risks for nonsyndromic cleft lip with or without cleft palate in newborns at a university hospital from West Mexico

scientific article published on 19 February 2018

Protective in vivo effect of curcumin on copper genotoxicity evaluated by comet and micronucleus assays

scientific article published in January 2007

Report and review of the fetal brain disruption sequence

scientific article

Unusual retrospective prenatal findings in a male newborn with Timothy syndrome type 1.

scientific article published on 13 April 2015

Variantes fenotípicas menores en pacientes con leucemia linfoblástica aguda del occidente de México

[Dermatoglyphics differences among children with nephrotic syndrome according to steroid response].

scientific article published in March 2016

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