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List of works by María De Lourdes Ramirez-Dueñas

1,2:3,4-Diepoxybutane Induces Multipolar Mitosis in Cultured Human Lymphocytes

scientific article published on 19 May 2016

A 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24

scientific article published on 01 January 2007

Alphoidless centromere of a familial unstable inverted Y chromosome

scientific article published on 01 January 1996

Are the faciothoracoskeletal syndrome and the Guadalajara camptodactyly syndrome type I distinct entities?

scientific article published on 01 September 1995

Assignment of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridization

scientific article published on 01 January 2000

Assignment of karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridization

scientific article published on 01 January 2000

Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

scientific article

Autosomal recessive spondylo-epi-metaphyseal dysplasia (Irapa type) in a Mexican family: delineation of the syndrome

scientific article published on 01 January 1980

Benign familial macrocephaly in a mother-son pair

scientific article published on 01 January 2010

Bosma arrhinia microphthalmia syndrome in a Mexican patient with a molecular analysis of PAX6.

scientific article published in January 2016

Caudal duplication: case report

scientific article published in July 2012

Expanding the phenotype of spondylospinal thoracic dysostosis (the Turkel-Chen-Johnson syndrome)

scientific article published on 01 January 2015

Family history of handedness and language problems in Mexican reading-disabled children

scientific article published on 01 January 1996

Floating-Harbor syndrome. A neuropsychological approach

scientific article published on 01 January 1996

Gestational diabetes mellitus and congenital malformations

scientific article published in October 2001

Guadalajara camptodactyly syndrome type I. A corroborative family.

scientific article published in January 1993

Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome.

scientific article published in October 2002

Hardy-Weinberg equilibrium analysis of the 48 bp VNTR in the III exon of the DRD4 gene in a sample of parents of ADHD cases

scientific article published on 2 June 2015

Hb Chiapas alpha 2 114 Pro replaced by Arg beta 2: identification by high pressure liquid chromatography

scientific article published on 01 January 1981

Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation

scientific article (publication date: August 1993)

Lujan syndrome in a Mexican boy.

scientific article

Methylenetetrahydrofolate reductase gene 677CT polymorphism and isolated congenital heart disease in a Mexican population.

scientific article published on 24 December 2011

Neuropsychological Impairment in School-Aged Children Born to Mothers With Gestational Diabetes.

scientific article published on 26 March 2015

Opposite imbalances of distal 14q in two unrelated patients

scientific article published on 01 January 1992

Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait.

scientific article published on January 2007

Severe Craniofacial Involvement due to Amniotic Band Sequence

scientific article published on 16 January 2018

Severe Silver-Russell syndrome and translocation (17;20) (q25;q13)

scientific article

Silent microcephaly: a distinct autosomal dominant trait.

scientific article published on April 1983

Silver-Russell syndrome and exclusion of uniparental disomy

scientific article published on 01 December 1996

Spondyloepimetaphyseal dysplasia (SEMD) Shohat type

scientific article published on 01 July 1994

Syntactic processing in Turner's syndrome

scientific article published on 01 September 2002

The variable phenotype in tetrasomy 18p syndrome. A propos of a subtle dysmorphic case

scientific article published on January 1, 2010

True hermaphroditism and sequences. Diagnostic implications regarding two cases

scientific article published in September 2008

Two different Philadelphia chromosomes in a cell line from an AML-M0 patient ⬇️

scientific article published on October 15, 1997

Zimmermann-Laband syndrome: further clinical delineation.

scientific article published in January 2005

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