A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).
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Abnormalities, Multiple↗
Biomedical subjects
R L Neu
Publications and source records attributed to R L Neu.
48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosome.
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Adult↗
An adult phenotypic male with a 46,XX chromosome complement.
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Adult↗
Lysergide and cannabis as possible teratogens in man.
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Abnormalities, Drug-Induced↗
Triple (45,X-46,XXr-46,XX) mosaicism in a phenotypic female.
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Adolescent↗
Testicular agenesis in a boy with XY-XYY mosaicism.
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Child↗
D-D translocation (XY, D-, t(DqDq)+) in a body with mental retardation and congenital dislocation of the hip.
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Abnormalities, Multiple↗
Disappearance of a 47,XX,C+ leucocyte cell line in an infant who had previously exhibited 46,XX-47,XX,C+ mosaicism.
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Abnormalities, Multiple↗
Octocentric human ring chromosome (Xr): proposed mechanism of formation.
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Cheek↗
Chromosome abnormalities in lymph node cells from patient with familial lymphoma. Loss of No. 3 chromosome and presence of large submetacentric chromosome in reticulum cell sarcoma tissue.
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Aged↗
45,X-46,XXp-mosaicism in a prepubertal girl.
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Autoradiography↗
XY-XYY mosaicism in prepubertal boy with tall stature, prognathism, and malformations of the hands.
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Body Height↗
New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.
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Autoradiography↗
Fibroblast chromosome preparations.
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Fibroblasts↗
Cri-du-chat syndrome in a 10 year old girl with deletion of the short arms of chromosome number 5. Observations on dermatoglyphics, maxillo-mandibular measurements and sound spectrograms.
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Anthropometry↗