Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: A clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata

Human Genetics

Volumn 97, Issue 5, 1996, Pages 564-567

  Hasegawa, Tomonobu ^a   Ogata, Tsutomu ^d   Hasegawa, Yukihiro ^a   Honda, Masataka ^b   Nagai, Toshiro ^c   Fukushima, Yoshimitsu ^e   Nakahori, Yutaka ^f   Matsuo, Nobutake ^d  

^a Div of Endocrinology and Metabolism   (Japan)

^b Division of Nephrology   (Japan)

^c Division of Neurology   (Japan)

^d KEIO UNIVERSITY   (Japan)

^e SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AORTA COARCTATION; ARTICLE; CASE REPORT; GENE MUTATION; HUMAN; HUMAN CELL; JAPAN; KARYOTYPE 46,XY; KIDNEY HYPOPLASIA; LYMPHATIC SYSTEM; MALE; NOONAN SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; TURNER SYNDROME;

AORTIC COARCTATION; CELL LINE; CHILD; FEMALE; GENETIC MARKERS; HUMANS; KARYOTYPING; KIDNEY; LYMPHOCYTES; MALE; MUTATION; NOONAN SYNDROME; POLYMERASE CHAIN REACTION; TURNER SYNDROME; X CHROMOSOME; Y CHROMOSOME;

EID: 0029930189     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02281861     Document Type: Article

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