Literature DB >> 4820908

Cytogenetics of fifty patients with primary amenorrhea.

G E Sarto.   

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Year:  1974        PMID： 4820908     DOI： 10.1016/0002-9378(74)90312-3

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN： 0002-9378            Impact factor:   8.661


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  10 in total

1.  Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11).

Authors:  S Stengel-Rutkowski; H Zankl; A Rodewald; S Scharrer; J P Chaudhuri; K D Zang
Journal:  Hum Genet       Date:  1976-01-28       Impact factor: 4.132

2.  BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

Authors:  S A Latt; H F Willard; P S Gerald
Journal:  Chromosoma       Date:  1976-08-17       Impact factor: 4.316

3.  Abnormal X chromosomes in man: origin, behavior and effects.

Authors:  E Therman; K Patau
Journal:  Humangenetik       Date:  1974

4.  Cytogenetic investigations in 150 cases with complaints of sterility or primary amenorrhea.

Authors:  A Joseph; I M Thomas
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

5.  The buccal smear: Reassessment of its usefulness.

Authors:  H A Gardner
Journal:  Can Med Assoc J       Date:  1976-03-20       Impact factor: 8.262

6.  Cytogenic investigation of 103 patients with primary or secondary amenorrhea.

Authors:  O Opitz; B Zoll; I Hansmann; B Hinney
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

Review 7.  The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches.

Authors:  Daniel Guerrier; Thomas Mouchel; Laurent Pasquier; Isabelle Pellerin
Journal:  J Negat Results Biomed       Date:  2006-01-27

Review 8.  Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.

Authors:  Karine Morcel; Laure Camborieux; Daniel Guerrier
Journal:  Orphanet J Rare Dis       Date:  2007-03-14       Impact factor: 4.123

9.  [Mayer-Rokitansky-Küster-Hauser syndrome: a cause of primary amenorrhea: about a case].

Authors:  Mohamed Abdellaoui; Jamal El Fenni; Meryem Edderai
Journal:  Pan Afr Med J       Date:  2021-12-23

10.  Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

Authors:  Agnès Burel; Thomas Mouchel; Sylvie Odent; Filiz Tiker; Bertrand Knebelmann; Isabelle Pellerin; Daniel Guerrier
Journal:  J Negat Results Biomed       Date:  2006-03-23
  10 in total

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