PMID: 2237479Oct 1, 1990Paper

Nonimmune hydrops fetalis: a heterogeneous disorder and therapeutic challenge

Seminars in Roentgenology
P Samuels, J Ludmir


No abstract listed.


Aug 1, 1978·Journal of Clinical Ultrasound : JCU·J M PriceJ Jacobson
Feb 1, 1978·Journal of Clinical Ultrasound : JCU·P Defoort, M Thiery
Dec 1, 1979·Southern Medical Journal·H R Boer, G Anido
May 1, 1989·Obstetrics and Gynecology·J S SamraG Constantine
Jun 1, 1989·Obstetrical & Gynecological Survey·M M CohenK J Blakemore
Jun 1, 1989·Journal of Pediatric Surgery·M T LongakerM R Harrison
Jul 1, 1989·Obstetrical & Gynecological Survey·F E HarlassJ Read
Jul 1, 1987·Infection·T F SchwarzF Deinhardt
Apr 1, 1988·Journal of Clinical Pathology·H J PorterK A Fleming
Feb 8, 1986·Lancet·K H NicolaidesC M Gosden
Mar 5, 1988·Lancet·M J AndersonW J Smith
Jul 1, 1987·The Journal of Infectious Diseases·C H WoernleJ M Davison
Nov 1, 1988·Archives of Disease in Childhood·V ChawlaF K Nkrumah
Oct 1, 1987·American Journal of Obstetrics and Gynecology·P D MillerD N Marinoff
Feb 4, 1988·The New England Journal of Medicine·F DaffosW L Cox
Oct 1, 1986·American Journal of Obstetrics and Gynecology·R A CastilloD Geist
Nov 1, 1987·American Journal of Obstetrics and Gynecology·J S Younis, M Granat
Jan 1, 1985·Acta Obstetricia Et Gynecologica Scandinavica·A J JaffaM R Peyser
Feb 1, 1986·Obstetrics and Gynecology·R NakayamaR W Hale
Mar 1, 1986·British Journal of Obstetrics and Gynaecology·L D AllanM G Chapman
Mar 1, 1986·British Journal of Obstetrics and Gynaecology·J D GoughP J Iliff
Jan 1, 1973·Nephron·N HallmanJ Rapola
Jul 1, 1969·The Journal of Pediatrics·R A ArcillaK Ranniger
Aug 1, 1984·The Journal of Hygiene·M J AndersonB J Cohen
Dec 1, 1984·European Journal of Pediatrics·M BeckJ Gehler
Feb 3, 1983·The New England Journal of Medicine·M Lubinsky, P Rapoport
Oct 1, 1984·Journal of Adolescent Health Care : Official Publication of the Society for Adolescent Medicine·P C LeppertM N Yeh
Mar 1, 1984·American Journal of Obstetrics and Gynecology·S S ImR J Benzie
Jun 1, 1984·Radiology·B S MahonyM S Golbus
May 1, 1983·British Journal of Obstetrics and Gynaecology·R A Fay
Nov 1, 1995·Archives of Disease in Childhood. Fetal and Neonatal Edition·N SuzukiM Inoue
Dec 1, 1956·The Journal of Obstetrics and Gynaecology of the British Empire·A D BAINW F FLINT


Apr 8, 1998·British Journal of Haematology·T WunF Tablin
Sep 11, 2010·Neonatal Network : NN·Andrea L Randenberg
Nov 13, 2010·Neonatal Network : NN·Andrea L Randenberg
Aug 2, 2003·Revista do Hospital das Clínicas·Renata Suman MascarettiCléa Rodrigues Leone
Dec 13, 1997·Journal of Pediatric Surgery·J F BealerD W Tuggle

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