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A de novo interstitial 6q deletion in a boy with a split hand malformation
(Journal of Applied Genetics 48(4), 2007, pp. 405-407, 2015)
Interstitial long-arm deletion of chromosome 7 and ectrodactyly
(1989-01-01)
An interstitial deletion of 7q21 was found in a boy with mental retardation, microcephaly, convergent strabismus, micrognathia, genital anomalies, and other findings, including ectrodactyly.
Interstitial long-arm deletion of chromosome 7 and ectrodactyly
(1989-01-01)
An interstitial deletion of 7q21 was found in a boy with mental retardation, microcephaly, convergent strabismus, micrognathia, genital anomalies, and other findings, including ectrodactyly.
8p23.1 Interstitial Deletion In A Patient With Congenital Cardiopathy, Neurobehavioral Disorders, And Minor Signs Suggesting 22q11.2 Deletion Syndrome
(LIPPINCOTT WILLIAMS & WILKINSPHILADELPHIA, 2015)
Similar interstitial deletions of the KAL-1 gene in two Brazilian families with X-linked Kallmann Syndrome
(Sociedade Brasileira de Genética, 2004)
A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state
(ELSEVIER SCIENCE BVAMSTERDAM, 2012)
Submicroscopic chromosomal anomalies play an important role in the etiology of craniofacial malformations, including midline facial defects with hypertelorism (MFDH). MFDH is a common feature combination in several conditions, ...
Cytogenomic Delineation and Clinical Follow-up of Two Siblings with an 8.5 Mb 6q24.2-q25.2 Deletion Inherited From a Paternal Insertion
(Wiley-Blackwell, 2014-09-01)
The chromosomal segment 6q24-q25 comprises a contiguous gene microdeletion syndrome characterized by intrauterine growth retardation, growth delay, intellectual disability, cardiac anomalies, and a dysmorphic facial ...