Published December, 2022
By Brij Kishore Tyagi
Publisher: Springer (Springer Verlag, Singapore)
Rating: 1.00
Availability: Available

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Published December, 2022
By Rekha Gurunath Rao
Publisher: Independent Self Publisher
Rating: 1.00
Availability: Available

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Published December, 2022
By Thomas Liehr
Publisher: Taylor & Francis
Rating: 1.00
Availability: Available

Genomic technologies provide the means of diagnosis and management of many human diseases. Without insights from cytogenetics, correct interpretation of modern high throughput results is difficult, if not impossible.

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Published December, 2022
By Mujeeb Zafar Banday, Saniya Nissar and Syed Sameer Aga
Publisher: Taylor & Francis
Rating: 1.00
Availability: Available

Genetic polymorphisms are important determinants of phenotypic variations and may modulate the risk to or even cause various diseases including genetic disorders and multifactorial diseases.

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Published December, 2022
By Ritobrata Goswami and Chandra S. Boosani
Publisher: Elsevier (Academic Press Inc)
Rating: 1.00
Availability: Available

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Published December, 2022
By Jennifer B. Mccormick and Jyotishman Pathak
Publisher: Elsevier (Academic Press Inc)
Rating: 1.00
Availability: Available

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Published November, 2022
By Rudolf Happle and Antonio Torrelo
Publisher: Springer (Springer Nature Switzerland AG)
Rating: 1.00
Availability: Available

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Published November, 2022
By Panayiotis Vlamos
Publisher: Springer (Springer Nature Switzerland AG)
Rating: 1.00
Availability: Available

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Published November, 2022
By Jaroslava Halper
Publisher: Springer (Springer Nature Switzerland AG)
Rating: 1.00
Availability: Available

This volume represents a substantially revised and updated 2nd edition of a reference handbook on major structural components of soft connective tissues and a whole slew of heritable diseases of soft connective tissues.

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Published November, 2022
By Toshifumi Yokota and Rika Maruyama
Publisher: Springer (Springer-Verlag New York Inc.)
Rating: 1.00
Availability: Contact supplier

This detailed book presents a comprehensive collection of state-of-the-art protocols on muscular dystrophy therapeutics, covering therapeutics using antisense oligonucleotides, gene replacement, genome editing, small molecules, stem cells, and antibodies.

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