Abbas N - Search Results

1

Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.

Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M. Abbas N, et al. C R Acad Sci III. 1993;316(4):375-83. C R Acad Sci III. 1993. PMID: 8402263

2

A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY.

McElreavey K, Rappaport R, Vilain E, Abbas N, Richaud F, Lortat-Jacob S, Berger R, Le Coniat M, Boucekkine C, Kucheria K, et al. McElreavey K, et al. Among authors: abbas n. Hum Genet. 1992 Sep-Oct;90(1-2):121-5. doi: 10.1007/BF00210754. Hum Genet. 1992. PMID: 1427767

3

A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development.

McElreavey K, Vilain E, Abbas N, Herskowitz I, Fellous M. McElreavey K, et al. Among authors: abbas n. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3368-72. doi: 10.1073/pnas.90.8.3368. Proc Natl Acad Sci U S A. 1993. PMID: 8475082 Free PMC article.

4

A possible common origin of "Y-negative" human XX males and XX true hermaphrodites.

Abbas NE, Toublanc JE, Boucekkine C, Toublanc M, Affara NA, Job JC, Fellous M. Abbas NE, et al. Hum Genet. 1990 Mar;84(4):356-60. doi: 10.1007/BF00196234. Hum Genet. 1990. PMID: 2307458

5

The sole presence of the testis-determining region of the Y chromosome (SRY) in 46,XX patients is associated with phenotypic variability.

Boucekkine C, Toublanc JE, Abbas N, Semrouni M, Vilain E, McElreavey K, Mugneret F, Fellous M. Boucekkine C, et al. Among authors: abbas n. Horm Res. 1992;37(6):236-40. doi: 10.1159/000182319. Horm Res. 1992. PMID: 1292977

6

XY sex reversal associated with a deletion 5' to the SRY "HMG box" in the testis-determining region.

McElreavy K, Vilain E, Abbas N, Costa JM, Souleyreau N, Kucheria K, Boucekkine C, Thibaud E, Brauner R, Flamant F, et al. McElreavy K, et al. Among authors: abbas n. Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):11016-20. doi: 10.1073/pnas.89.22.11016. Proc Natl Acad Sci U S A. 1992. PMID: 1438307 Free PMC article.

7

[Genetic factor of sex determination].

Abbas N, Toublanc J, Rappaport R, Fekete-Nihoul C, Boucekine C, Chabouni H, Fellous M. Abbas N, et al. Bull Assoc Anat (Nancy). 1991 Mar;75(228):7-14. Bull Assoc Anat (Nancy). 1991. PMID: 1782471 Review. French.

8

A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1.

Abbas N, Novelli G, Stella NC, Triolo O, Corrado F, Fellous M, Chery M, Gilgenkrantz S, Dallapiccola B. Abbas N, et al. Hum Genet. 1990 Nov;86(1):94-8. doi: 10.1007/BF00205184. Hum Genet. 1990. PMID: 2253943

9

Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation.

Toublanc JE, Boucekkine C, Abbas N, Barama D, Vilain E, McElreavey K, Toublanc M, Fellous M. Toublanc JE, et al. Among authors: abbas n. Eur J Pediatr. 1993;152 Suppl 2:S70-5. doi: 10.1007/BF02125443. Eur J Pediatr. 1993. PMID: 8339747

10

Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences.

Boucekkine C, Toublanc JE, Abbas N, Chaabouni S, Ouahid S, Semrouni M, Jaubert F, Toublanc M, McElreavey K, Vilain E, et al. Boucekkine C, et al. Among authors: abbas n. Clin Endocrinol (Oxf). 1994 Jun;40(6):733-42. doi: 10.1111/j.1365-2265.1994.tb02506.x. Clin Endocrinol (Oxf). 1994. PMID: 8033363

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