April 2021 - Volume 30 - Issue 2 - Contributor Index

Alphabetical Search
I
N
O
Q
U
X
Y
Author:
Adir, Noam

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Adir, V.

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Aykut, Ayca

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Chinta, Navya
Author:
Chudley, Albert
Author:
Cogulu, Dilsah
Author:
Cogulu, Ozgur
Author:
Dori, Yoav
Author:
Dubey, Sudhisha
Author:
Durmaz, Asude
Author:
Elley, George
Author:
Frosk, Patrick
Author:
Ghosh, Apurba

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Goobie, Sharan
Author:
Gowda, Mamatha
Author:
Hovanes, Karine

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Jezela-Stanek, Aleksandra; Pokora, Paulina; Mlynek, Marlena; More

Clinical Dysmorphology. 30(2):76-82, April 2021.

Author:
Kurolap, Alina

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Larom-Khan, G.

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Li, Dong
Author:
Lim, Derek
Author:
Liu, Jing
Author:
Marles, Sandra
Author:
Mercer, Leanne
Author:
Mhanni, Aziz
Author:
Mlynek, Marlena

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Jezela-Stanek, Aleksandra; Pokora, Paulina; Mlynek, Marlena; More

Clinical Dysmorphology. 30(2):76-82, April 2021.

Author:
Mohan, Shruthi
Author:
Mojarrab, Neda
Author:
Mory, Adi

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Paperna, Tamar

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Peleg, Amir

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Pokora, Paulina

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Jezela-Stanek, Aleksandra; Pokora, Paulina; Mlynek, Marlena; More

Clinical Dysmorphology. 30(2):76-82, April 2021.

Author:
Prasad, Chitra
Author:
Puri, Ratna Dua
Author:
Ramesh, Devika

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Jezela-Stanek, Aleksandra; Pokora, Paulina; Mlynek, Marlena; More

Clinical Dysmorphology. 30(2):76-82, April 2021.

Author:
Sabir, Ataf H.
Author:
Sagi-Dain, Lena

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Sandal, Sapna
Author:
Saxena, Renu
Author:
Schanze, Denny
Author:
Shuldiner, A.R.

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Singh, Ananya
Author:
Sloman, Melissa
Author:
Smyk, Marta

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Jezela-Stanek, Aleksandra; Pokora, Paulina; Mlynek, Marlena; More

Clinical Dysmorphology. 30(2):76-82, April 2021.

Author:
Traub, Eric S.

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Jezela-Stanek, Aleksandra; Pokora, Paulina; Mlynek, Marlena; More

Clinical Dysmorphology. 30(2):76-82, April 2021.

Author:
Velsher, Lea
Author:
Verma, Jyotsna
Author:
Wollstein, R.

A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1

Peleg, Amir; Kurolap, Alina; Sagi-Dain, Lena; More

Clinical Dysmorphology. 30(2):71-75, April 2021.

Author:
Zenker, Martin

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Jezela-Stanek, Aleksandra; Pokora, Paulina; Mlynek, Marlena; More

Clinical Dysmorphology. 30(2):76-82, April 2021.

Show: