[Cases of congenital malformations of children of consanguineous couples]. 1969

B Farza, and M Chelli, and A Rebel

UI MeSH Term Description Entries
D008297 Male Males
D009008 Abnormalities, Severe Teratoid Marked developmental anomalies of a fetus or infant. Abnormality, Severe Teratoid,Severe Teratoid Abnormalities,Severe Teratoid Abnormality,Teratoid Abnormalities, Severe,Teratoid Abnormality, Severe
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D003241 Consanguinity The magnitude of INBREEDING in humans. Inbreeding, Human,Consanguineous Marriage,Consanguinous Mating,Consanguineous Marriages,Consanguinities,Consanguinous Matings,Human Inbreeding,Human Inbreedings,Inbreedings, Human,Marriage, Consanguineous,Marriages, Consanguineous,Mating, Consanguinous,Matings, Consanguinous
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities
D014428 Twins, Conjoined MONOZYGOTIC TWINS who are joined in utero. They may be well developed and share only a superficial connection, often in the frontal, transverse or sagittal body plane, or they may share a partial duplication of a body structure. Alternatively, there may be a small and incompletely developed twin conjoined to a larger, more fully developed twin. Siamese Twins,Twins, Siamese,Conjoined Twin,Conjoined Twins,Siamese Twin,Twin, Conjoined,Twin, Siamese

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