[Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)]

Abilities and needs of children with genetic syndromes.

Genetic counseling (Geneva, Switzerland)·2006

Physical and developmental phenotype analyses in a boy with Wolf-Hirschhorn syndrome.

Genetic counseling (Geneva, Switzerland)·2005

A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).

Cytogenetics and cell genetics·2001

[Are you prescribing fatal hormones? Bremen professor accuses physicians with unsubstantiated claims].

MMW Fortschritte der Medizin·2001

Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.

Annales de genetique·1999

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.

Nature genetics·1998

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study.

Frontiers in genetics·2026

GRIA3 Duplication at Xq25 in a Young Adult Male With Profound Intellectual Disability and Morbid Obesity: A Case Report.

Case reports in genetics·2026

Leveraging Long-Read Sequencing to Bridge the Diagnostic and Equity Gaps in Differences of Sex Development (DSD).

The Journal of clinical endocrinology and metabolism·2026

Progenitor Timing Shapes NG2-Glia Fate and Oligodendrocyte Differentiation.

Glia·2026

Fraternal Birth Order Effect and Other Sibship Effects in Bisexual and Asexual Men and Women.

Archives of sexual behavior·2026

Correlation analysis of cognitive dysfunction and fluctuations in serum fibroblast growth factor 21 (FGF21) levels in the overweight group.

Journal of medical biochemistry·2026

Related Experiment Videos

[Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)]

Related Concept Videos

Abilities and needs of children with genetic syndromes.

Physical and developmental phenotype analyses in a boy with Wolf-Hirschhorn syndrome.

A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).

[Are you prescribing fatal hormones? Bremen professor accuses physicians with unsubstantiated claims].

Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study.

GRIA3 Duplication at Xq25 in a Young Adult Male With Profound Intellectual Disability and Morbid Obesity: A Case Report.

Leveraging Long-Read Sequencing to Bridge the Diagnostic and Equity Gaps in Differences of Sex Development (DSD).

Progenitor Timing Shapes NG2-Glia Fate and Oligodendrocyte Differentiation.

Fraternal Birth Order Effect and Other Sibship Effects in Bisexual and Asexual Men and Women.

Correlation analysis of cognitive dysfunction and fluctuations in serum fibroblast growth factor 21 (FGF21) levels in the overweight group.

Related Experiment Videos

[Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)]

Related Concept Videos

Related Articles