Results 181 to 190 of about 468,507 (253)
CUX1 variant and 9p deletion: expanding the spectrum and resolving variable GDD/ID in a family. [PDF]
BMC Med GenomicsLiu H +12 more
europepmc +1 more source
Case Report: Post-LASIK exacerbation of granular corneal dystrophy type 2: a familial case with <i>TGFBI</i> mutation. [PDF]
Front Med (Lausanne)Kuang L +6 more
europepmc +1 more source
Typical presentation of autosomal recessive oculocutaneous albinism in two siblings. [PDF]
GMS Ophthalmol CasesNishant P, Aftab N, Saha B, Raj A.
europepmc +1 more source
Early genetic events in the colorectal carcinogenic pathway of familial adenomatous polyposis and sporadic polyp: germline and somatic alterations in carcinogenesis. [PDF]
Front GenetTanabe H +13 more
europepmc +1 more source
The Family History and the Pedigree Chart
Postgraduate Medicine, 1972 In investigating the etiology of a familial disease, it is important to obtain a detailed family history and to construct a pedigree chart. The chart not only aids in recognizing genetic factors in the disease but also provides important information for genetic counseling.
Hymie Gordon
semanticscholar +4 more sources
The pedigree chart analysis of centenarians in Shanghai City
Archives of Gerontology and Geriatrics, 1993 The sex, occupation and pedigree charts of 57 centenarians in Shanghai City were investigated. There were 10 (17.5%) males and 47 (82.5%) females. Of the males, 4 were office workers (40%) and 6 were manual workers (60%). Among the females, 1 was an office worker (2.1%), 3 were manual workers (6.4%) and 43 were housewives (91.5%).
Yuan Chaohui +6 more
semanticscholar +4 more sources
Commentary: Gender Identity Inclusive Pedigree Chart for High School Biology
The Science Teacher, 2022 Sal Kaczowska, Susan Groziak
semanticscholar +3 more sources