PMID: 14399877Dec 12, 1959Paper

The chromosomes in a case of pure gonadal dysgenesis

British Medical Journal
D G HARNDEN, J S STEWART

Abstract

No abstract listed.

References

Sep 17, 1955·British Medical Journal·G I SWYER
Apr 11, 1959·Nature·C E FORDP M BISHOP
Aug 1, 1959·The Journal of Clinical Endocrinology and Metabolism·G A ELLIOTTD RABINOWITZ
Oct 17, 1959·Lancet·P A JACOBSB LENNOX
Sep 5, 1959·Lancet·I M NILSSONJ WALDENSTROM

Citations

May 25, 1963·Canadian Medical Association Journal·K L Moore, J C Hay
Apr 1, 1961·The American Journal of Medicine·S I GRIBOFF, R LAWRENCE
May 1, 1970·Journal of Biosocial Science. Supplement·C E FORD
Nov 24, 1960·The New England Journal of Medicine·K HIRSCHHORNH L COOPER
May 27, 1965·The New England Journal of Medicine·M M COHEN, M W SHAW
Apr 16, 1970·The New England Journal of Medicine·H L JuddB Kliman
Nov 18, 1997·Acta Paediatrica Japonica; Overseas Edition·A K TemoçinU Zorludemir
Jun 1, 1976·Journal of Medical Genetics·S K AlfaroG Pérez-Palacios
Dec 1, 1967·Journal of Medical Genetics·P E Ferrier, V C Kelley
Jun 1, 1984·Journal of Endocrinological Investigation·C BoucekkineM Bachammar
Aug 1, 1970·Archives of Disease in Childhood·C J DEWHURST
Dec 1, 1973·Australian and New Zealand Journal of Medicine·E J KeoghM G Fitzgerald
Jun 1, 1967·The Journal of Obstetrics and Gynaecology of the British Commonwealth·C J DEWHURST
Feb 1, 1962·The Journal of Obstetrics and Gynaecology of the British Empire·W M BROWN, T N MACGREGOR
Aug 1, 1963·The Journal of Obstetrics and Gynaecology of the British Commonwealth·C J DEWHURSTC E BLANK
May 1, 1964·The Journal of Pediatrics·S D FRASIERH D MOSIER
Jan 1, 1979·American Journal of Medical Genetics·J M Opitz, P D Pallister
Jan 1, 1979·American Journal of Medical Genetics·H R NazarethM C Lima
Feb 1, 1968·The Journal of Obstetrics and Gynaecology of the British Commonwealth·D J BartlettW Aherne
Dec 1, 1966·The British Journal of Psychiatry : the Journal of Mental Science·J Nielsen, N Thomsen
Jan 1, 1968·Archiv für Gynäkologie·O FettigJ Schneider
Jun 19, 1964·Archiv für Gynäkologie·H J STAEMMLERH BREHM
Jan 1, 1978·International Journal of Gynaecology and Obstetrics : the Official Organ of the International Federation of Gynaecology and Obstetrics·J A Fayez
Jan 1, 1968·Archiv für Gynäkologie·R A PFEIFFERJ Ruckes
Jan 1, 1968·Archiv für Gynäkologie·H Naujoks, H J Pallaske
May 15, 1965·Klinische Wochenschrift·R A PFEIFFERI SCHLUETER
Jun 1, 1961·Klinische Wochenschrift·C OVERZIER
Jan 1, 1961·Postgraduate Medicine·D J PATANELLI, W O NELSON

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