Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns

[Measuring pressure pain thresholds. Comparison of an electromechanically controlled algometer with established methods].

Schmerz (Berlin, Germany)·2007

[The role of MRI in suspected inner ear malformations].

RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin·2003

Weekly carboplatin and docetaxel for locally advanced primary and recurrent cervical cancer: a phase I study.

Gynecologic oncology·2002

Prophylactic intravenous hydroxyethyle starch solution prevents moderate-severe ovarian hyperstimulation in in-vitro fertilization patients: a prospective, randomized, double-blind and placebo-controlled study.

Human reproduction (Oxford, England)·1998

[Intracytoplasmic injection (ICSI) of cryopreserved testicular spermatozoa (Cryo-TESE): a retrospective study of the first 250 treatment cycles].

Zentralblatt fur Gynakologie·1998

Gender differences in fat mass of 5-7-year old children.

International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity·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

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

International journal of legal medicine·2026

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

Phlebology·2026

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Cytogenetic and genome research·2026

Cognitive flexibility deficits differ between the sexes in a transchromosomic mouse model of Down syndrome.

Disease models & mechanisms·2026

Compromised striatal structure and function in mouse models of RARB-related disorder.

Brain : a journal of neurology·2026

Defective neuronal differentiation in Lowe syndrome is associated with mitochondrial dysfunction and impaired cilia-related Sonic Hedgehog signaling.

eLife·2026

Related Experiment Videos

Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns

Related Concept Videos

[Measuring pressure pain thresholds. Comparison of an electromechanically controlled algometer with established methods].

[The role of MRI in suspected inner ear malformations].

Weekly carboplatin and docetaxel for locally advanced primary and recurrent cervical cancer: a phase I study.

Prophylactic intravenous hydroxyethyle starch solution prevents moderate-severe ovarian hyperstimulation in in-vitro fertilization patients: a prospective, randomized, double-blind and placebo-controlled study.

[Intracytoplasmic injection (ICSI) of cryopreserved testicular spermatozoa (Cryo-TESE): a retrospective study of the first 250 treatment cycles].

Gender differences in fat mass of 5-7-year old children.

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.

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Cognitive flexibility deficits differ between the sexes in a transchromosomic mouse model of Down syndrome.

Compromised striatal structure and function in mouse models of RARB-related disorder.

Defective neuronal differentiation in Lowe syndrome is associated with mitochondrial dysfunction and impaired cilia-related Sonic Hedgehog signaling.

Related Experiment Videos

Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns

Related Concept Videos

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