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Publications by M Shaham

Clinical Features and Mental Development of a Child With a Prenatally Identified 45,XX,der(5)t(5;18) (P15;q11.2),-18 Karyotype.

Journal of Medical Genetics

English

Related publications

A 14 Year-Old Girl With Turner Syndrome of Complicated Karyotype; 45,x/47,XY,+18,−19,+der(19),t(Y;19)(q12;p13.3)

Japanese journal of human genetics

English

Maternal Uniparental Disomy 12 in a Healthy Girl With a 47,XX,+der(12)(:p11->q11:)/46,xx Karyotype

Journal of Medical Genetics

English

A Child With 45,x/46,X,del(Y)(q12) Identified With a Y-Specific Probe

Fertility and Sterility

Reproductive Medicine

English

A Patient With 45,XX,Gminus-46,XX,Gr Mosaicism.

Journal of Medical Genetics

English

46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China

Frontiers in Genetics

Molecular Medicine

English

Down's Syndrome Associated With Two Robertsonian Translocations, 45,xx,-15,-21,+t(15q21q) and 46,xx,-21,+t(21q21q)

Journal of Medical Genetics

English

T(2;22)(p23;q11.2)

Atlas of Genetics and Cytogenetics in Oncology and Haematology

Cancer Research

English

T(4;22)(q12;q11.2)

Atlas of Genetics and Cytogenetics in Oncology and Haematology

Cancer Research

English

A De Novo Complex Chromosomal Rearrangement of 46,XX,t(7;15;13)(p15;q21;q31) in a Female With an Adverse Obstetric History

International Journal of Human Genetics

English