Participation of D-group chromosomes in satelite associations

Novel (CA)n marker DXYS241 on the nonrecombinant part of the human Y chromosome.

Human biology·1999

Polymerase chain reaction analysis of the Y chromosome long arm in azoospermic patients: lack of the Y chromosome recognition motif (YRRM1) gene.

International journal of urology : official journal of the Japanese Urological Association·1998

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.

Nature·1998

YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.

Genomics·1997

A novel (CA)n polymorphism on 6p21.1-21.2.

The Japanese journal of human genetics·1996

Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.

American journal of human genetics·1996

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

Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.

Hormone research in paediatrics·2026

Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.

Frontiers in behavioral neuroscience·2026

A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46, XY Siblings With Ambiguous Genitalia: A Case Series.

Clinical case reports·2026

The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).

Wellcome open research·2026

The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).

Wellcome open research·2026

Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.

The Journal of molecular diagnostics : JMD·2026

Related Experiment Videos

Participation of D-group chromosomes in satelite associations

Related Concept Videos

Novel (CA)n marker DXYS241 on the nonrecombinant part of the human Y chromosome.

Polymerase chain reaction analysis of the Y chromosome long arm in azoospermic patients: lack of the Y chromosome recognition motif (YRRM1) gene.

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.

YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.

A novel (CA)n polymorphism on 6p21.1-21.2.

Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.

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.

Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.

Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.

A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46, XY Siblings With Ambiguous Genitalia: A Case Series.

The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).

The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).

Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.

Related Experiment Videos

Participation of D-group chromosomes in satelite associations

Related Concept Videos

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