Annales de Genetique

Hyperphenylalaninemia and birth weight
pp. 105-107(3)
Authors: Bianca S.; Meli C.; Barrano B.; Mollica F.

Mutation screening of the muscarinic m2 and m3 receptor genes in asthmatics, outgrow subjects, and normal controls
pp. 109-113(5)
Authors: Yamamoto T.; Yamashita N.; Kuwabara M.; Nakano J.; Sugimoto H.; Akiyama K.; Hirai K.; Ishii A.; Uehara Y.; Ohta K.

Impact of prenatal diagnosis on livebirth prevalence of children with congenital anomalies
pp. 115-121(7)
Authors: Stoll C.; Alembik Y.; Dott B.; Roth M.P.

Non-allelic heterogeneity in familial unilateral renal adysplasia
pp. 123-126(4)
Authors: Li Volti S.; Faiella A.; Perrotta S.; Li Volti G.; Lama G.; Bianca S.; Boncinelli E.

Distal trisomy 10q and limb defects
pp. 127-129(3)
Author: Lurie I.W.

Cytogenetic survey of 117 Tunisian patients with de novo myelodysplastic syndrome
pp. 131-135(5)
Authors: Sendi H.S.; Hichri H.; Elghezal H.; Gribaa M.; Laatiri A.; Elloumi M.; Lakhal R.B.; Saad A.

A complex mosaicism 45,X/46,X,del(Xq)/46,X,idic(Xq) in a patient with secondary amenorrhea
pp. 137-140(4)
Authors: Calvano S.; de Cillis G.P.; Croce A.I.; Perla G.; Notarangelo A.; Zelante L.

Prenatal detection of a paracentric inversion 16(q11.2q13)
pp. 141-142(2)
Authors: Perez C.; Lloveras E.; Zamora L.; Melero C.; Perez E.; Plaja A.

Partial trisomy of distal 5q and partial monosomy of Xp as a result of mating between two translocation carriers: a female with a balanced translocation t(X;5)(p11;q31) and a male with a der(13;14)(q10;q10)-a case report and a family study
pp. 143-146(4)
Authors: Wysocka B.; Brozek I.; Wierzba J.; Kardas I.; Wozniak A.; Kowalczyk J.; Balcerska A.; Limon J.

A cytogenetic study of Kuwaiti couples with infertility and reproductive disorders: short arm deletion of chromosome 21 is associated with male infertility
pp. 147-149(3)
Authors: Alkhalaf M.; Verghese L.; Muharib N.

Severe bone changes in a case of Hutchinson-Gilford syndrome
pp. 151-155(5)
Authors: de Paula Rodrigues G.H.; Tamega I.d.E.; Duque G.; Spinola Dias Neto V.

Endoreduplication of the hyperhaploid maternal complement and abnormal pronuclear formation in a human zygote obtained after intracytoplasmic sperm injection
pp. 157-159(3)
Authors: Rosenbusch B.; Glaeser B.; Brucker C.; Schneider M.

Ring chromosome 8 and translocation t(8;21) in a patient with acute myeloblastic leukemia
pp. 161-163(3)
Authors: Berger R.; Busson M.

TPA stimulation culture for improved detection of t(11;14)(q13;q32) in mantle cell lymphoma
pp. 165-168(4)
Authors: Barouk-Simonet E.; Andrieux J.; Copin M.-C.; Grardel-Duflos N.; Huyghe P.; Patte J.-H.; Preudhomme C.; Quesnel B.; Lai J.-L.